ClinVar Miner

List of variants in gene combination LOC107303340, VHL reported as likely benign for not provided

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Total variants: 19
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HGVS dbSNP
NM_000551.3(VHL):c.341-182C>T rs552624308
NM_000551.3(VHL):c.341-216C>T rs143057620
NM_000551.3(VHL):c.341-4A>T rs1559428033
NM_000551.3(VHL):c.426T>C (p.Val142=) rs143594610
NM_000551.3(VHL):c.463+4C>T rs879253989
NM_000551.3(VHL):c.540C>T (p.Ile180=) rs374927292
NM_000551.3(VHL):c.549G>T (p.Ser183=) rs193922614
NM_000551.3(VHL):c.618T>C (p.Ile206=) rs1575932691
NM_000551.3(VHL):c.639T>C (p.Asp213=) rs775624944
NM_000551.4(VHL):c.366A>C (p.Ala122=) rs1474241640
NM_000551.4(VHL):c.387G>C (p.Leu129=) rs778846471
NM_000551.4(VHL):c.432A>G (p.Gly144=) rs1575928044
NM_000551.4(VHL):c.463+8C>T rs5030834
NM_000551.4(VHL):c.471T>C (p.Thr157=) rs1252473811
NM_000551.4(VHL):c.516T>G (p.Pro172=) rs1575932227
NM_000551.4(VHL):c.576A>C (p.Pro192=) rs1372952726
NM_000551.4(VHL):c.591C>T (p.Asp197=) rs1575932584
NM_000551.4(VHL):c.606A>C (p.Thr202=) rs1575932637
NM_000551.4(VHL):c.630G>A (p.Arg210=) rs1575932755

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