Split (1)

train · 1.23k rows

Unnamed: 0.1 int64 0 1.63k	Unnamed: 0 int64 0 1.63k	#AlleleID int64 27.4k 3.4M	Name stringlengths 25 43	GeneSymbol stringclasses 1 value	Chromosome int64 17 17	Start int64 7.67M 7.69M	Stop int64 7.67M 7.69M	ClinicalSignificance stringclasses 8 values	ReferenceAlleleVCF stringclasses 4 values	AlternateAlleleVCF stringclasses 4 values	IsPathogenic bool 2 classes	Strand stringclasses 1 value	NewIndex int64 99 19.6k
1,014	1,014	653,040	NM_000546.6(TP53):c.375+1G>C	TP53	17	7,675,993	7,675,993	Pathogenic/Likely pathogenic	C	G	true	reverse	11,497
643	643	432,943	NM_000546.6(TP53):c.375+2T>C	TP53	17	7,675,992	7,675,992	Pathogenic/Likely pathogenic	A	G	true	reverse	11,498
737	737	479,359	NM_000546.6(TP53):c.375+2T>G	TP53	17	7,675,992	7,675,992	Pathogenic/Likely pathogenic	A	C	true	reverse	11,498
872	872	531,833	NM_000546.6(TP53):c.375+2T>A	TP53	17	7,675,992	7,675,992	Pathogenic/Likely pathogenic	A	T	true	reverse	11,498
1,043	1,043	776,422	NM_000546.6(TP53):c.375+8G>T	TP53	17	7,675,986	7,675,986	Likely benign	C	A	false	reverse	11,504
1,490	1,490	2,080,888	NM_000546.6(TP53):c.375+8G>C	TP53	17	7,675,986	7,675,986	Likely benign	C	G	false	reverse	11,504
1,492	1,492	2,085,947	NM_000546.6(TP53):c.375+11C>T	TP53	17	7,675,983	7,675,983	Likely benign	G	A	false	reverse	11,507
1,348	1,348	1,612,938	NM_000546.6(TP53):c.375+12T>C	TP53	17	7,675,982	7,675,982	Likely benign	A	G	false	reverse	11,508
544	544	376,707	NM_000546.6(TP53):c.375+13G>A	TP53	17	7,675,981	7,675,981	Likely benign	C	T	false	reverse	11,509
1,485	1,485	2,064,324	NM_000546.6(TP53):c.375+16G>T	TP53	17	7,675,978	7,675,978	Likely benign	C	A	false	reverse	11,512
543	543	376,705	NM_000546.6(TP53):c.375+16G>A	TP53	17	7,675,978	7,675,978	Likely benign	C	T	false	reverse	11,512
1,294	1,294	1,380,709	NM_000546.6(TP53):c.375+17G>T	TP53	17	7,675,977	7,675,977	Likely benign	C	A	false	reverse	11,513
389	389	358,965	NM_000546.6(TP53):c.375+17G>A	TP53	17	7,675,977	7,675,977	Likely benign	C	T	false	reverse	11,513
942	942	619,768	NM_000546.6(TP53):c.375+18G>A	TP53	17	7,675,976	7,675,976	Likely benign	C	T	false	reverse	11,514
1,600	1,600	3,025,210	NM_000546.6(TP53):c.375+18G>T	TP53	17	7,675,976	7,675,976	Likely benign	C	A	false	reverse	11,514
1,482	1,482	2,057,053	NM_000546.6(TP53):c.375+19C>G	TP53	17	7,675,975	7,675,975	Likely benign	G	C	false	reverse	11,515
1,536	1,536	2,741,148	NM_000546.6(TP53):c.375+49G>A	TP53	17	7,675,945	7,675,945	Likely benign	C	T	false	reverse	11,545
1,023	1,023	685,438	NM_000546.6(TP53):c.376-283T>C	TP53	17	7,675,519	7,675,519	Benign	A	G	false	reverse	11,971
1,269	1,269	1,228,189	NM_000546.6(TP53):c.376-161A>G	TP53	17	7,675,397	7,675,397	Benign	T	C	false	reverse	12,093
1,273	1,273	1,235,465	NM_000546.6(TP53):c.376-125T>C	TP53	17	7,675,361	7,675,361	Benign	A	G	false	reverse	12,129
1,022	1,022	669,358	NM_000546.6(TP53):c.376-117G>A	TP53	17	7,675,353	7,675,353	Likely benign	C	T	false	reverse	12,137
1,283	1,283	1,309,574	NM_000546.6(TP53):c.376-101A>T	TP53	17	7,675,337	7,675,337	Benign	T	A	false	reverse	12,153
644	644	433,983	NM_000546.6(TP53):c.376-91G>A	TP53	17	7,675,327	7,675,327	Benign	C	T	false	reverse	12,163
1,020	1,020	669,112	NM_000546.6(TP53):c.376-86T>C	TP53	17	7,675,322	7,675,322	Likely benign	A	G	false	reverse	12,168
1,462	1,462	1,859,936	NM_000546.6(TP53):c.376-24T>A	TP53	17	7,675,260	7,675,260	Likely benign	A	T	false	reverse	12,230
784	784	485,151	NM_000546.6(TP53):c.376-20T>C	TP53	17	7,675,256	7,675,256	Likely benign	A	G	false	reverse	12,234
532	532	376,613	NM_000546.6(TP53):c.376-19C>T	TP53	17	7,675,255	7,675,255	Likely benign	G	A	false	reverse	12,235
542	542	376,704	NM_000546.6(TP53):c.376-17C>T	TP53	17	7,675,253	7,675,253	Benign/Likely benign	G	A	false	reverse	12,237
1,298	1,298	1,398,780	NM_000546.6(TP53):c.376-16C>T	TP53	17	7,675,252	7,675,252	Likely benign	G	A	false	reverse	12,238
1,614	1,614	3,228,766	NM_000546.6(TP53):c.376-15T>C	TP53	17	7,675,251	7,675,251	Likely benign	A	G	false	reverse	12,239
1,163	1,163	916,582	NM_000546.6(TP53):c.376-14T>G	TP53	17	7,675,250	7,675,250	Likely benign	A	C	false	reverse	12,240
1,162	1,162	916,579	NM_000546.6(TP53):c.376-13C>T	TP53	17	7,675,249	7,675,249	Likely benign	G	A	false	reverse	12,241
1,469	1,469	1,958,800	NM_000546.6(TP53):c.376-12C>T	TP53	17	7,675,248	7,675,248	Likely benign	G	A	false	reverse	12,242
1,334	1,334	1,586,171	NM_000546.6(TP53):c.376-11T>G	TP53	17	7,675,247	7,675,247	Likely benign	A	C	false	reverse	12,243
1,313	1,313	1,520,656	NM_000546.6(TP53):c.376-10C>T	TP53	17	7,675,246	7,675,246	Likely benign	G	A	false	reverse	12,244
1,245	1,245	1,147,708	NM_000546.6(TP53):c.376-8T>G	TP53	17	7,675,244	7,675,244	Likely benign	A	C	false	reverse	12,246
854	854	506,428	NM_000546.6(TP53):c.376-7C>T	TP53	17	7,675,243	7,675,243	Likely benign	G	A	false	reverse	12,247
1,566	1,566	2,911,132	NM_000546.6(TP53):c.376-7C>A	TP53	17	7,675,243	7,675,243	Likely benign	G	T	false	reverse	12,247
222	222	185,392	NM_000546.6(TP53):c.376-2A>G	TP53	17	7,675,238	7,675,238	Pathogenic/Likely pathogenic	T	C	true	reverse	12,252
688	688	469,166	NM_000546.6(TP53):c.376-2A>T	TP53	17	7,675,238	7,675,238	Pathogenic/Likely pathogenic	T	A	true	reverse	12,252
736	736	479,357	NM_000546.6(TP53):c.376-1G>A	TP53	17	7,675,237	7,675,237	Pathogenic/Likely pathogenic	C	T	true	reverse	12,253
1,530	1,530	2,739,571	NM_000546.6(TP53):c.376-1G>C	TP53	17	7,675,237	7,675,237	not provided	C	G	false	reverse	12,253
1,264	1,264	1,200,292	NM_000546.6(TP53):c.376-1G>T	TP53	17	7,675,237	7,675,237	Pathogenic	C	A	true	reverse	12,253
1,302	1,302	1,451,155	NM_000546.6(TP53):c.378C>A (p.Tyr126Ter)	TP53	17	7,675,234	7,675,234	Pathogenic	G	T	true	reverse	12,256
906	906	574,637	NM_000546.6(TP53):c.378C>G (p.Tyr126Ter)	TP53	17	7,675,234	7,675,234	Pathogenic/Likely pathogenic	G	C	true	reverse	12,256
1,142	1,142	914,198	NM_000546.6(TP53):c.378C>T (p.Tyr126=)	TP53	17	7,675,234	7,675,234	Likely benign	G	A	false	reverse	12,256
1,175	1,175	938,240	NM_000546.6(TP53):c.379T>C (p.Ser127Pro)	TP53	17	7,675,233	7,675,233	Pathogenic/Likely pathogenic	A	G	true	reverse	12,257
1,004	1,004	646,767	NM_000546.6(TP53):c.380C>A (p.Ser127Tyr)	TP53	17	7,675,232	7,675,232	Pathogenic	G	T	true	reverse	12,258
282	282	222,742	NM_000546.6(TP53):c.380C>G (p.Ser127Cys)	TP53	17	7,675,232	7,675,232	Pathogenic	G	C	true	reverse	12,258
1,343	1,343	1,605,137	NM_000546.6(TP53):c.381C>T (p.Ser127=)	TP53	17	7,675,231	7,675,231	Likely benign	G	A	false	reverse	12,259
1,244	1,244	1,147,707	NM_000546.6(TP53):c.381C>A (p.Ser127=)	TP53	17	7,675,231	7,675,231	Likely benign	G	T	false	reverse	12,259
1,374	1,374	1,790,008	NM_000546.6(TP53):c.384T>A (p.Pro128=)	TP53	17	7,675,228	7,675,228	Likely benign	A	T	false	reverse	12,262
709	709	479,285	NM_000546.6(TP53):c.384T>C (p.Pro128=)	TP53	17	7,675,228	7,675,228	Likely benign	A	G	false	reverse	12,262
70	70	137,019	NM_000546.6(TP53):c.386C>T (p.Ala129Val)	TP53	17	7,675,226	7,675,226	not provided	G	A	false	reverse	12,264
1,375	1,375	1,790,163	NM_000546.6(TP53):c.386C>A (p.Ala129Asp)	TP53	17	7,675,226	7,675,226	Benign	G	T	false	reverse	12,264
1,371	1,371	1,786,943	NM_000546.6(TP53):c.387C>T (p.Ala129=)	TP53	17	7,675,225	7,675,225	Likely benign	G	A	false	reverse	12,265
1,085	1,085	814,500	NM_000546.6(TP53):c.389T>A (p.Leu130His)	TP53	17	7,675,223	7,675,223	Pathogenic	A	T	true	reverse	12,267
636	636	420,666	NM_000546.6(TP53):c.389T>C (p.Leu130Pro)	TP53	17	7,675,223	7,675,223	Pathogenic	A	G	true	reverse	12,267
221	221	185,391	NM_000546.6(TP53):c.390C>T (p.Leu130=)	TP53	17	7,675,222	7,675,222	Likely benign	G	A	false	reverse	12,268
112	112	151,702	NM_000546.6(TP53):c.391A>T (p.Asn131Tyr)	TP53	17	7,675,221	7,675,221	Pathogenic	T	A	true	reverse	12,269
635	635	420,665	NM_000546.6(TP53):c.392A>T (p.Asn131Ile)	TP53	17	7,675,220	7,675,220	Pathogenic/Likely pathogenic	T	A	true	reverse	12,270
1,141	1,141	914,197	NM_000546.6(TP53):c.393C>T (p.Asn131=)	TP53	17	7,675,219	7,675,219	Likely benign	G	A	false	reverse	12,271
1,487	1,487	2,070,928	NM_000546.6(TP53):c.394A>T (p.Lys132Ter)	TP53	17	7,675,218	7,675,218	Pathogenic	T	A	true	reverse	12,272
454	454	363,504	NM_000546.6(TP53):c.395A>G (p.Lys132Arg)	TP53	17	7,675,217	7,675,217	Pathogenic/Likely pathogenic	T	C	true	reverse	12,273
972	972	622,631	NM_000546.6(TP53):c.396G>T (p.Lys132Asn)	TP53	17	7,675,216	7,675,216	Pathogenic/Likely pathogenic	C	A	true	reverse	12,274
453	453	363,503	NM_000546.6(TP53):c.396G>C (p.Lys132Asn)	TP53	17	7,675,216	7,675,216	Likely pathogenic	C	G	true	reverse	12,274
10	10	27,396	NM_000546.6(TP53):c.398T>C (p.Met133Thr)	TP53	17	7,675,214	7,675,214	Pathogenic	A	G	true	reverse	12,276
1,512	1,512	2,403,662	NM_000546.6(TP53):c.398T>A (p.Met133Lys)	TP53	17	7,675,214	7,675,214	Likely pathogenic	A	T	true	reverse	12,276
726	726	479,343	NM_000546.6(TP53):c.400T>A (p.Phe134Ile)	TP53	17	7,675,212	7,675,212	Pathogenic/Likely pathogenic	A	T	true	reverse	12,278
327	327	236,493	NM_000546.6(TP53):c.401T>G (p.Phe134Cys)	TP53	17	7,675,211	7,675,211	Likely pathogenic	A	C	true	reverse	12,279
802	802	485,328	NM_000546.6(TP53):c.402T>C (p.Phe134=)	TP53	17	7,675,210	7,675,210	Likely benign	A	G	false	reverse	12,280
400	400	363,442	NM_000546.6(TP53):c.403T>G (p.Cys135Gly)	TP53	17	7,675,209	7,675,209	Likely pathogenic	A	C	true	reverse	12,281
398	398	363,439	NM_000546.6(TP53):c.403T>C (p.Cys135Arg)	TP53	17	7,675,209	7,675,209	Pathogenic/Likely pathogenic	A	G	true	reverse	12,281
397	397	363,438	NM_000546.6(TP53):c.404G>T (p.Cys135Phe)	TP53	17	7,675,208	7,675,208	Pathogenic/Likely pathogenic	C	A	true	reverse	12,282
724	724	479,338	NM_000546.6(TP53):c.405C>T (p.Cys135=)	TP53	17	7,675,207	7,675,207	Likely benign	G	A	false	reverse	12,283
1,370	1,370	1,784,620	NM_000546.6(TP53):c.406C>T (p.Gln136Ter)	TP53	17	7,675,206	7,675,206	Pathogenic	G	A	true	reverse	12,284
220	220	185,389	NM_000546.6(TP53):c.408A>G (p.Gln136=)	TP53	17	7,675,204	7,675,204	Benign/Likely benign	T	C	false	reverse	12,286
1,373	1,373	1,787,670	NM_000546.6(TP53):c.409C>T (p.Leu137=)	TP53	17	7,675,203	7,675,203	Likely benign	G	A	false	reverse	12,287
1,471	1,471	2,008,008	NM_000546.6(TP53):c.411G>A (p.Leu137=)	TP53	17	7,675,201	7,675,201	Likely benign	C	T	false	reverse	12,289
326	326	236,492	NM_000546.6(TP53):c.411G>C (p.Leu137=)	TP53	17	7,675,201	7,675,201	Likely benign	C	G	false	reverse	12,289
25	25	27,415	NM_000546.6(TP53):c.412G>C (p.Ala138Pro)	TP53	17	7,675,200	7,675,200	Pathogenic/Likely pathogenic	C	G	true	reverse	12,290
734	734	479,354	NM_000546.6(TP53):c.414C>T (p.Ala138=)	TP53	17	7,675,198	7,675,198	Likely benign	G	A	false	reverse	12,292
971	971	622,630	NM_000546.6(TP53):c.415A>T (p.Lys139Ter)	TP53	17	7,675,197	7,675,197	Pathogenic	T	A	true	reverse	12,293
403	403	363,445	NM_000546.6(TP53):c.421T>G (p.Cys141Gly)	TP53	17	7,675,191	7,675,191	Likely pathogenic	A	C	true	reverse	12,299
404	404	363,446	NM_000546.6(TP53):c.421T>A (p.Cys141Ser)	TP53	17	7,675,191	7,675,191	Likely pathogenic	A	T	true	reverse	12,299
84	84	150,515	NM_000546.6(TP53):c.422G>A (p.Cys141Tyr)	TP53	17	7,675,190	7,675,190	Pathogenic/Likely pathogenic	C	T	true	reverse	12,300
401	401	363,443	NM_000546.6(TP53):c.423C>G (p.Cys141Trp)	TP53	17	7,675,189	7,675,189	Pathogenic/Likely pathogenic	G	C	true	reverse	12,301
1,489	1,489	2,079,183	NM_000546.6(TP53):c.423C>T (p.Cys141=)	TP53	17	7,675,189	7,675,189	Likely benign	G	A	false	reverse	12,301
1,577	1,577	2,939,138	NM_000546.6(TP53):c.426T>C (p.Pro142=)	TP53	17	7,675,186	7,675,186	Likely benign	A	G	false	reverse	12,304
1,057	1,057	792,574	NM_000546.6(TP53):c.428T>C (p.Val143Ala)	TP53	17	7,675,184	7,675,184	Likely pathogenic	A	G	true	reverse	12,306
1,562	1,562	2,903,155	NM_000546.6(TP53):c.429G>A (p.Val143=)	TP53	17	7,675,183	7,675,183	Likely benign	C	T	false	reverse	12,307
970	970	622,629	NM_000546.6(TP53):c.430C>T (p.Gln144Ter)	TP53	17	7,675,182	7,675,182	Pathogenic	G	A	true	reverse	12,308
217	217	185,383	NM_000546.6(TP53):c.432G>A (p.Gln144=)	TP53	17	7,675,180	7,675,180	Likely benign	C	T	false	reverse	12,310
216	216	185,382	NM_000546.6(TP53):c.433C>T (p.Leu145=)	TP53	17	7,675,179	7,675,179	Likely benign	G	A	false	reverse	12,311
1,630	1,630	3,385,596	NM_000546.6(TP53):c.435G>A (p.Leu145=)	TP53	17	7,675,177	7,675,177	Likely benign	C	T	false	reverse	12,313
969	969	622,628	NM_000546.6(TP53):c.437G>A (p.Trp146Ter)	TP53	17	7,675,175	7,675,175	Pathogenic	C	T	true	reverse	12,315
634	634	420,663	NM_000546.6(TP53):c.438G>A (p.Trp146Ter)	TP53	17	7,675,174	7,675,174	Pathogenic	C	T	true	reverse	12,316
1,360	1,360	1,646,853	NM_000546.6(TP53):c.447C>T (p.Ser149=)	TP53	17	7,675,165	7,675,165	Likely benign	G	A	false	reverse	12,325
268	268	213,400	NM_000546.6(TP53):c.450A>G (p.Thr150=)	TP53	17	7,675,162	7,675,162	Likely benign	T	C	false	reverse	12,328
1,470	1,470	1,966,419	NM_000546.6(TP53):c.450A>T (p.Thr150=)	TP53	17	7,675,162	7,675,162	Likely benign	T	A	false	reverse	12,328

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