Datasets:

m42-health
/

tp53

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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
1,116	1,116	878,644	NM_000546.6(TP53):c.*357T>C	TP53	17	7,669,252	7,669,252	Likely benign	A	G	false	reverse	18,238
1,115	1,115	878,643	NM_000546.6(TP53):c.*409C>A	TP53	17	7,669,200	7,669,200	Likely benign	G	T	false	reverse	18,290
380	380	340,463	NM_000546.6(TP53):c.*485G>A	TP53	17	7,669,124	7,669,124	Benign	C	T	false	reverse	18,366
379	379	340,461	NM_000546.6(TP53):c.*613C>A	TP53	17	7,668,996	7,668,996	Benign	G	T	false	reverse	18,494
378	378	340,458	NM_000546.6(TP53):c.*773C>T	TP53	17	7,668,836	7,668,836	Benign	G	A	false	reverse	18,654
377	377	340,457	NM_000546.6(TP53):c.*826G>A	TP53	17	7,668,783	7,668,783	Benign	C	T	false	reverse	18,707
381	381	346,157	NM_000546.6(TP53):c.*936A>G	TP53	17	7,668,673	7,668,673	Likely benign	T	C	false	reverse	18,817
383	383	347,484	NM_000546.6(TP53):c.*1070C>T	TP53	17	7,668,539	7,668,539	Benign/Likely benign	G	A	false	reverse	18,951
1,613	1,613	3,220,717	NM_000546.6(TP53):c.*1169A>G	TP53	17	7,668,440	7,668,440	Likely benign	T	C	false	reverse	19,050
384	384	353,462	NM_001126113.2(TP53):c.*1422G>C	TP53	17	7,668,388	7,668,388	Likely benign	C	G	false	reverse	19,102
1,612	1,612	3,220,184	NC_000017.11:g.7668195G>A	TP53	17	7,668,195	7,668,195	Likely benign	G	A	false	reverse	19,295
1,611	1,611	3,215,283	NC_000017.11:g.7668194C>T	TP53	17	7,668,194	7,668,194	Likely benign	C	T	false	reverse	19,296
1,280	1,280	1,284,244	NC_000017.11:g.7668134G>A	TP53	17	7,668,134	7,668,134	Benign	G	A	false	reverse	19,356
1,131	1,131	914,173	NC_000017.11:g.7667933C>T	TP53	17	7,667,933	7,667,933	Likely benign	C	T	false	reverse	19,557
1,130	1,130	914,172	NC_000017.11:g.7667929C>T	TP53	17	7,667,929	7,667,929	Likely benign	C	T	false	reverse	19,561
1,129	1,129	914,171	NC_000017.11:g.7667926C>T	TP53	17	7,667,926	7,667,926	Likely benign	C	T	false	reverse	19,564
1,128	1,128	914,168	NC_000017.11:g.7667910C>A	TP53	17	7,667,910	7,667,910	Likely benign	C	A	false	reverse	19,580
1,127	1,127	914,167	NC_000017.11:g.7667909C>T	TP53	17	7,667,909	7,667,909	Likely benign	C	T	false	reverse	19,581
765	765	483,069	NM_000546.5(TP53):c.*1701G>T	TP53	17	7,667,908	7,667,908	Benign	C	A	false	reverse	19,582
1,125	1,125	914,165	NC_000017.11:g.7667906C>A	TP53	17	7,667,906	7,667,906	Likely benign	C	A	false	reverse	19,584
1,126	1,126	914,166	NC_000017.11:g.7667906C>T	TP53	17	7,667,906	7,667,906	Likely benign	C	T	false	reverse	19,584
1,124	1,124	914,164	NC_000017.11:g.7667904C>T	TP53	17	7,667,904	7,667,904	Likely benign	C	T	false	reverse	19,586
1,123	1,123	914,163	NC_000017.11:g.7667901C>T	TP53	17	7,667,901	7,667,901	Likely benign	C	T	false	reverse	19,589
1,122	1,122	914,162	NC_000017.11:g.7667899A>C	TP53	17	7,667,899	7,667,899	Likely benign	A	C	false	reverse	19,591
1,121	1,121	914,161	NC_000017.11:g.7667888G>A	TP53	17	7,667,888	7,667,888	Likely benign	G	A	false	reverse	19,602
1,120	1,120	914,160	NC_000017.11:g.7667880G>A	TP53	17	7,667,880	7,667,880	Likely benign	G	A	false	reverse	19,610
1,119	1,119	914,159	NC_000017.11:g.7667874G>C	TP53	17	7,667,874	7,667,874	Likely benign	G	C	false	reverse	19,616

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