ClinVar Miner

List of variants in gene DLC1 studied for cancer

Included ClinVar conditions (475):
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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_182643.3(DLC1):c.1530G>A (p.Ala510=) rs1127606 0.01715
NM_182643.3(DLC1):c.2199C>T (p.Ser733=) rs34941980 0.00252
NM_182643.3(DLC1):c.167A>G (p.Glu56Gly) rs143324598 0.00168
NM_182643.3(DLC1):c.2147T>C (p.Ile716Thr) rs114637912 0.00117
NM_182643.3(DLC1):c.1700C>T (p.Pro567Leu) rs139415835 0.00018
NM_182643.3(DLC1):c.2265G>C (p.Thr755=) rs138749997 0.00018
NM_182643.3(DLC1):c.3609C>A (p.Thr1203=) rs145989730 0.00008
NM_182643.3(DLC1):c.857A>G (p.Asn286Ser) rs374190119 0.00005
NM_182643.3(DLC1):c.1348+9A>C rs200908536 0.00002
NM_182643.3(DLC1):c.3327+8C>T rs559854315 0.00001
NM_182643.3(DLC1):c.2753G>C (p.Arg918Pro) rs779524261
NM_182643.3(DLC1):c.2875A>G (p.Thr959Ala) rs121908500

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