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
743	743	479,383	NM_000546.6(TP53):c.93T>G (p.Val31=)	TP53	17	7,676,385	7,676,385	Likely benign	A	C	false	reverse	11,105
1,421	1,421	1,821,503	NM_000546.6(TP53):c.94C>G (p.Leu32Val)	TP53	17	7,676,384	7,676,384	Likely benign	G	C	false	reverse	11,106
764	764	480,115	NM_000546.6(TP53):c.94C>T (p.Leu32=)	TP53	17	7,676,384	7,676,384	Likely benign	G	A	false	reverse	11,106
1,112	1,112	852,921	NM_000546.6(TP53):c.96+1G>A	TP53	17	7,676,381	7,676,381	Likely pathogenic	C	T	true	reverse	11,109
713	713	479,292	NM_000546.6(TP53):c.96+1G>T	TP53	17	7,676,381	7,676,381	Pathogenic/Likely pathogenic	C	A	true	reverse	11,109
638	638	420,679	NM_000546.6(TP53):c.96+1G>C	TP53	17	7,676,381	7,676,381	Pathogenic/Likely pathogenic	C	G	true	reverse	11,109
1,544	1,544	2,758,374	NM_000546.6(TP53):c.96+2T>G	TP53	17	7,676,380	7,676,380	Likely pathogenic	A	C	true	reverse	11,110
1,177	1,177	941,202	NM_000546.6(TP53):c.96+2T>A	TP53	17	7,676,380	7,676,380	Likely pathogenic	A	T	true	reverse	11,110
1,045	1,045	776,737	NM_000546.6(TP53):c.96+8C>G	TP53	17	7,676,374	7,676,374	Likely benign	G	C	false	reverse	11,116
1,250	1,250	1,147,713	NM_000546.6(TP53):c.96+9A>G	TP53	17	7,676,373	7,676,373	Likely benign	T	C	false	reverse	11,117
1,221	1,221	1,105,428	NM_000546.6(TP53):c.96+10A>G	TP53	17	7,676,372	7,676,372	Likely benign	T	C	false	reverse	11,118
1,572	1,572	2,931,371	NM_000546.6(TP53):c.96+11G>A	TP53	17	7,676,371	7,676,371	Likely benign	C	T	false	reverse	11,119
1,609	1,609	3,168,245	NM_000546.6(TP53):c.96+12G>A	TP53	17	7,676,370	7,676,370	Likely benign	C	T	false	reverse	11,120
1,585	1,585	2,982,241	NM_000546.6(TP53):c.96+13G>C	TP53	17	7,676,369	7,676,369	Likely benign	C	G	false	reverse	11,121
845	845	485,681	NM_000546.6(TP53):c.96+14T>C	TP53	17	7,676,368	7,676,368	Likely benign	A	G	false	reverse	11,122
1,481	1,481	2,056,496	NM_000546.6(TP53):c.96+17G>A	TP53	17	7,676,365	7,676,365	Likely benign	C	T	false	reverse	11,125
1,495	1,495	2,088,710	NM_000546.6(TP53):c.96+17G>T	TP53	17	7,676,365	7,676,365	Likely benign	C	A	false	reverse	11,125
1,364	1,364	1,670,813	NM_000546.6(TP53):c.96+41A>G	TP53	17	7,676,341	7,676,341	Likely benign	T	C	false	reverse	11,149
1,537	1,537	2,741,149	NM_000546.6(TP53):c.97-44G>A	TP53	17	7,676,316	7,676,316	Likely benign	C	T	false	reverse	11,174
373	373	256,464	NM_000546.6(TP53):c.97-29C>A	TP53	17	7,676,301	7,676,301	Benign	G	T	false	reverse	11,189
390	390	358,966	NM_000546.6(TP53):c.97-28T>A	TP53	17	7,676,300	7,676,300	Likely benign	A	T	false	reverse	11,190
1,328	1,328	1,559,599	NM_000546.6(TP53):c.97-19T>A	TP53	17	7,676,291	7,676,291	Likely benign	A	T	false	reverse	11,199
534	534	376,629	NM_000546.6(TP53):c.97-17T>C	TP53	17	7,676,289	7,676,289	Likely benign	A	G	false	reverse	11,201
889	889	539,382	NM_000546.6(TP53):c.97-15T>C	TP53	17	7,676,287	7,676,287	Likely benign	A	G	false	reverse	11,203
1,590	1,590	2,989,825	NM_000546.6(TP53):c.97-15T>G	TP53	17	7,676,287	7,676,287	Likely benign	A	C	false	reverse	11,203
1,017	1,017	653,531	NM_000546.6(TP53):c.97-11C>G	TP53	17	7,676,283	7,676,283	Pathogenic	G	C	true	reverse	11,207
533	533	376,616	NM_000546.6(TP53):c.97-11C>T	TP53	17	7,676,283	7,676,283	Likely benign	G	A	false	reverse	11,207
1,030	1,030	760,598	NM_000546.6(TP53):c.97-10C>T	TP53	17	7,676,282	7,676,282	Likely benign	G	A	false	reverse	11,208
835	835	485,524	NM_000546.6(TP53):c.97-8A>T	TP53	17	7,676,280	7,676,280	Likely benign	T	A	false	reverse	11,210
284	284	222,744	NM_000546.6(TP53):c.97-6C>T	TP53	17	7,676,278	7,676,278	Benign/Likely benign	G	A	false	reverse	11,212
1,044	1,044	776,735	NM_000546.6(TP53):c.97-4A>G	TP53	17	7,676,276	7,676,276	Likely benign	T	C	false	reverse	11,214
369	369	245,080	NM_000546.6(TP53):c.97-2A>G	TP53	17	7,676,274	7,676,274	Pathogenic	T	C	true	reverse	11,216
1,622	1,622	3,307,477	NM_000546.6(TP53):c.97-2A>C	TP53	17	7,676,274	7,676,274	Likely pathogenic	T	G	true	reverse	11,216
1,012	1,012	652,855	NM_000546.6(TP53):c.97-1G>A	TP53	17	7,676,273	7,676,273	Likely pathogenic	C	T	true	reverse	11,217
1,015	1,015	653,042	NM_000546.6(TP53):c.97-1G>T	TP53	17	7,676,273	7,676,273	Pathogenic/Likely pathogenic	C	A	true	reverse	11,217
1,096	1,096	814,520	NM_000546.6(TP53):c.102C>T (p.Pro34=)	TP53	17	7,676,267	7,676,267	Likely benign	G	A	false	reverse	11,223
243	243	185,415	NM_000546.6(TP53):c.102C>G (p.Pro34=)	TP53	17	7,676,267	7,676,267	Benign/Likely benign	G	C	false	reverse	11,223
1,616	1,616	3,229,869	NM_000546.6(TP53):c.103T>C (p.Leu35=)	TP53	17	7,676,266	7,676,266	Likely benign	A	G	false	reverse	11,224
129	129	152,276	NM_000546.6(TP53):c.105G>C (p.Leu35Phe)	TP53	17	7,676,264	7,676,264	Likely benign	C	G	false	reverse	11,226
21	21	27,410	NM_000546.6(TP53):c.105G>T (p.Leu35Phe)	TP53	17	7,676,264	7,676,264	Pathogenic	C	A	true	reverse	11,226
103	103	151,311	NM_000546.6(TP53):c.107C>A (p.Pro36Gln)	TP53	17	7,676,262	7,676,262	Likely benign	G	T	false	reverse	11,228
1,441	1,441	1,841,215	NM_000546.6(TP53):c.108G>T (p.Pro36=)	TP53	17	7,676,261	7,676,261	Likely benign	C	A	false	reverse	11,229
65	65	136,456	NM_000546.6(TP53):c.108G>A (p.Pro36=)	TP53	17	7,676,261	7,676,261	Benign	C	T	false	reverse	11,229
689	689	469,175	NM_000546.6(TP53):c.111C>T (p.Ser37=)	TP53	17	7,676,258	7,676,258	Likely benign	G	A	false	reverse	11,232
834	834	485,523	NM_000546.6(TP53):c.111C>G (p.Ser37=)	TP53	17	7,676,258	7,676,258	Likely benign	G	C	false	reverse	11,232
1,619	1,619	3,307,369	NM_000546.6(TP53):c.112C>T (p.Gln38Ter)	TP53	17	7,676,257	7,676,257	Pathogenic	G	A	true	reverse	11,233
1,054	1,054	785,764	NM_000546.6(TP53):c.117A>G (p.Ala39=)	TP53	17	7,676,252	7,676,252	Likely benign	T	C	false	reverse	11,238
242	242	185,414	NM_000546.6(TP53):c.123T>C (p.Asp41=)	TP53	17	7,676,246	7,676,246	Benign/Likely benign	A	G	false	reverse	11,244
1,025	1,025	727,460	NM_000546.6(TP53):c.126T>C (p.Asp42=)	TP53	17	7,676,243	7,676,243	Likely benign	A	G	false	reverse	11,247
1,410	1,410	1,818,338	NM_000546.6(TP53):c.127T>C (p.Leu43=)	TP53	17	7,676,242	7,676,242	Likely benign	A	G	false	reverse	11,248
649	649	445,904	NM_000546.6(TP53):c.128T>A (p.Leu43Ter)	TP53	17	7,676,241	7,676,241	Likely pathogenic	A	T	true	reverse	11,249
1,249	1,249	1,147,712	NM_000546.6(TP53):c.129G>A (p.Leu43=)	TP53	17	7,676,240	7,676,240	Likely benign	C	T	false	reverse	11,250
582	582	402,603	NM_000546.6(TP53):c.135G>A (p.Leu45=)	TP53	17	7,676,234	7,676,234	Likely benign	C	T	false	reverse	11,256
1,499	1,499	2,102,401	NM_000546.6(TP53):c.138C>T (p.Ser46=)	TP53	17	7,676,231	7,676,231	Likely benign	G	A	false	reverse	11,259
33	33	52,757	NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	TP53	17	7,676,230	7,676,230	Benign	G	A	false	reverse	11,260
1,211	1,211	1,083,633	NM_000546.6(TP53):c.141G>T (p.Pro47=)	TP53	17	7,676,228	7,676,228	Likely benign	C	A	false	reverse	11,262
241	241	185,413	NM_000546.6(TP53):c.141G>A (p.Pro47=)	TP53	17	7,676,228	7,676,228	Benign/Likely benign	C	T	false	reverse	11,262
345	345	236,513	NM_000546.6(TP53):c.144C>T (p.Asp48=)	TP53	17	7,676,225	7,676,225	Likely benign	G	A	false	reverse	11,265
88	88	150,770	NM_000546.6(TP53):c.144C>A (p.Asp48Glu)	TP53	17	7,676,225	7,676,225	Likely benign	G	T	false	reverse	11,265
240	240	185,412	NM_000546.6(TP53):c.145G>A (p.Asp49Asn)	TP53	17	7,676,224	7,676,224	Likely benign	C	T	false	reverse	11,266
78	78	139,660	NM_000546.6(TP53):c.145G>C (p.Asp49His)	TP53	17	7,676,224	7,676,224	Likely benign	C	G	false	reverse	11,266
239	239	185,411	NM_000546.6(TP53):c.147T>C (p.Asp49=)	TP53	17	7,676,222	7,676,222	Benign/Likely benign	A	G	false	reverse	11,268
273	273	213,405	NM_000546.6(TP53):c.149T>C (p.Ile50Thr)	TP53	17	7,676,220	7,676,220	Likely benign	A	G	false	reverse	11,270
897	897	571,660	NM_000546.6(TP53):c.151G>T (p.Glu51Ter)	TP53	17	7,676,218	7,676,218	Pathogenic	C	A	true	reverse	11,272
1,304	1,304	1,464,516	NM_000546.6(TP53):c.154C>T (p.Gln52Ter)	TP53	17	7,676,215	7,676,215	Pathogenic	G	A	true	reverse	11,275
558	558	378,809	NM_000546.6(TP53):c.156A>G (p.Gln52=)	TP53	17	7,676,213	7,676,213	Likely benign	T	C	false	reverse	11,277
343	343	236,511	NM_000546.6(TP53):c.158G>A (p.Trp53Ter)	TP53	17	7,676,211	7,676,211	Pathogenic	C	T	true	reverse	11,279
618	618	410,283	NM_000546.6(TP53):c.159G>A (p.Trp53Ter)	TP53	17	7,676,210	7,676,210	Pathogenic	C	T	true	reverse	11,280
1,234	1,234	1,126,813	NM_000546.6(TP53):c.165T>G (p.Thr55=)	TP53	17	7,676,204	7,676,204	Likely benign	A	C	false	reverse	11,286
1,285	1,285	1,320,111	NM_000546.6(TP53):c.166G>T (p.Glu56Ter)	TP53	17	7,676,203	7,676,203	Likely pathogenic	C	A	true	reverse	11,287
272	272	213,404	NM_000546.6(TP53):c.168A>G (p.Glu56=)	TP53	17	7,676,201	7,676,201	Likely benign	T	C	false	reverse	11,289
1,437	1,437	1,834,492	NM_000546.6(TP53):c.170A>T (p.Asp57Val)	TP53	17	7,676,199	7,676,199	Likely benign	T	A	false	reverse	11,291
740	740	479,372	NM_000546.6(TP53):c.171C>T (p.Asp57=)	TP53	17	7,676,198	7,676,198	Likely benign	G	A	false	reverse	11,292
1,434	1,434	1,831,528	NM_000546.6(TP53):c.172C>G (p.Pro58Ala)	TP53	17	7,676,197	7,676,197	Likely benign	G	C	false	reverse	11,293
604	604	403,164	NM_000546.6(TP53):c.174A>G (p.Pro58=)	TP53	17	7,676,195	7,676,195	Likely benign	T	C	false	reverse	11,295
1,094	1,094	814,517	NM_000546.6(TP53):c.176G>A (p.Gly59Asp)	TP53	17	7,676,193	7,676,193	Likely benign	C	T	false	reverse	11,297
1,438	1,438	1,838,620	NM_000546.6(TP53):c.177T>A (p.Gly59=)	TP53	17	7,676,192	7,676,192	Likely benign	A	T	false	reverse	11,298
238	238	185,409	NM_000546.6(TP53):c.180A>C (p.Pro60=)	TP53	17	7,676,189	7,676,189	Benign/Likely benign	T	G	false	reverse	11,301
1,435	1,435	1,831,834	NM_000546.6(TP53):c.180A>G (p.Pro60=)	TP53	17	7,676,189	7,676,189	Likely benign	T	C	false	reverse	11,301
1,286	1,286	1,320,112	NM_000546.6(TP53):c.183T>C (p.Asp61=)	TP53	17	7,676,186	7,676,186	Likely benign	A	G	false	reverse	11,304
908	908	608,821	NM_000546.6(TP53):c.184G>T (p.Glu62Ter)	TP53	17	7,676,185	7,676,185	Pathogenic	C	A	true	reverse	11,305
342	342	236,510	NM_000546.6(TP53):c.187G>A (p.Ala63Thr)	TP53	17	7,676,182	7,676,182	Likely benign	C	T	false	reverse	11,308
169	169	181,027	NM_000546.6(TP53):c.188C>T (p.Ala63Val)	TP53	17	7,676,181	7,676,181	Likely benign	G	A	false	reverse	11,309
341	341	236,509	NM_000546.6(TP53):c.188C>G (p.Ala63Gly)	TP53	17	7,676,181	7,676,181	Likely benign	G	C	false	reverse	11,309
1,210	1,210	1,083,632	NM_000546.6(TP53):c.189T>C (p.Ala63=)	TP53	17	7,676,180	7,676,180	Likely benign	A	G	false	reverse	11,310
663	663	467,555	NM_000546.6(TP53):c.192C>G (p.Pro64=)	TP53	17	7,676,177	7,676,177	Likely benign	G	C	false	reverse	11,313
1,615	1,615	3,229,868	NM_000546.6(TP53):c.192C>T (p.Pro64=)	TP53	17	7,676,177	7,676,177	Likely benign	G	A	false	reverse	11,313
977	977	622,651	NM_000546.6(TP53):c.193A>T (p.Arg65Ter)	TP53	17	7,676,176	7,676,176	Pathogenic	T	A	true	reverse	11,314
763	763	480,112	NM_000546.6(TP53):c.193A>C (p.Arg65=)	TP53	17	7,676,176	7,676,176	Likely benign	T	G	false	reverse	11,314
1,053	1,053	785,763	NM_000546.6(TP53):c.195A>G (p.Arg65=)	TP53	17	7,676,174	7,676,174	Likely benign	T	C	false	reverse	11,316
1,440	1,440	1,839,674	NM_000546.6(TP53):c.196A>G (p.Met66Val)	TP53	17	7,676,173	7,676,173	Likely benign	T	C	false	reverse	11,317
237	237	185,408	NM_000546.6(TP53):c.201A>G (p.Pro67=)	TP53	17	7,676,168	7,676,168	Likely benign	T	C	false	reverse	11,322
286	286	226,368	NM_000546.6(TP53):c.202G>T (p.Glu68Ter)	TP53	17	7,676,167	7,676,167	Pathogenic	C	A	true	reverse	11,323
236	236	185,407	NM_000546.6(TP53):c.204G>A (p.Glu68=)	TP53	17	7,676,165	7,676,165	Likely benign	C	T	false	reverse	11,325
283	283	222,743	NM_000546.6(TP53):c.207T>C (p.Ala69=)	TP53	17	7,676,162	7,676,162	Likely benign	A	G	false	reverse	11,328
235	235	185,406	NM_000546.6(TP53):c.210T>C (p.Ala70=)	TP53	17	7,676,159	7,676,159	Likely benign	A	G	false	reverse	11,331
603	603	403,162	NM_000546.6(TP53):c.210T>A (p.Ala70=)	TP53	17	7,676,159	7,676,159	Likely benign	A	T	false	reverse	11,331
858	858	506,757	NM_000546.6(TP53):c.213C>T (p.Pro71=)	TP53	17	7,676,156	7,676,156	Likely benign	G	A	false	reverse	11,334
4	4	27,390	NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	TP53	17	7,676,154	7,676,154	Benign	G	C	false	reverse	11,336
234	234	185,405	NM_000546.6(TP53):c.215C>A (p.Pro72His)	TP53	17	7,676,154	7,676,154	Likely benign	G	T	false	reverse	11,336

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