ClinVar Miner

List of variants in gene VARS2 reported as uncertain significance by Ambry Genetics

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_020442.6(VARS2):c.1168G>A (p.Ala390Thr) rs202201763 0.00039
NM_020442.6(VARS2):c.23C>A (p.Ser8Tyr) rs145694863 0.00034
NM_020442.6(VARS2):c.2624C>T (p.Pro875Leu) rs376070793 0.00028
NM_020442.6(VARS2):c.787C>T (p.Arg263Trp) rs200002496 0.00026
NM_020442.6(VARS2):c.2495C>T (p.Ser832Leu) rs138341222 0.00012
NM_020442.6(VARS2):c.3092T>G (p.Leu1031Arg) rs201946203 0.00006
NM_020442.6(VARS2):c.1163C>T (p.Thr388Met) rs140305500 0.00005
NM_020442.6(VARS2):c.1496C>G (p.Ala499Gly) rs751016666 0.00005
NM_020442.6(VARS2):c.142C>G (p.Gln48Glu) rs750590170 0.00004
NM_020442.6(VARS2):c.3091-6G>A rs753415520 0.00004
NM_020442.6(VARS2):c.1484T>G (p.Val495Gly) rs759325866 0.00003
NM_020442.6(VARS2):c.2831C>G (p.Ala944Gly) rs747655762 0.00003
NM_020442.6(VARS2):c.104A>G (p.His35Arg) rs199534441 0.00002
NM_020442.6(VARS2):c.2683C>T (p.Arg895Cys) rs1258140939 0.00001
NM_020442.6(VARS2):c.3031G>C (p.Asp1011His) rs139921739 0.00001
NM_020442.6(VARS2):c.-28+114G>T
NM_020442.6(VARS2):c.-28+120G>A
NM_020442.6(VARS2):c.-28+89C>T rs948200308
NM_020442.6(VARS2):c.1063T>C (p.Ser355Pro)
NM_020442.6(VARS2):c.1064C>T (p.Ser355Leu)
NM_020442.6(VARS2):c.1073C>T (p.Thr358Ile) rs1554267386
NM_020442.6(VARS2):c.1081C>T (p.His361Tyr)
NM_020442.6(VARS2):c.1097G>A (p.Arg366His)
NM_020442.6(VARS2):c.1490C>T (p.Ser497Leu)
NM_020442.6(VARS2):c.14C>A (p.Pro5His)
NM_020442.6(VARS2):c.1596G>T (p.Gln532His)
NM_020442.6(VARS2):c.1615G>A (p.Val539Ile)
NM_020442.6(VARS2):c.1615G>C (p.Val539Leu)
NM_020442.6(VARS2):c.1646G>A (p.Cys549Tyr)
NM_020442.6(VARS2):c.1700C>T (p.Thr567Ile)
NM_020442.6(VARS2):c.251A>T (p.Tyr84Phe)
NM_020442.6(VARS2):c.2563C>G (p.Pro855Ala)
NM_020442.6(VARS2):c.2609C>A (p.Pro870His)
NM_020442.6(VARS2):c.2701C>T (p.Arg901Trp)
NM_020442.6(VARS2):c.2728G>A (p.Val910Met)
NM_020442.6(VARS2):c.2776C>T (p.Arg926Trp)
NM_020442.6(VARS2):c.298C>G (p.Leu100Val)
NM_020442.6(VARS2):c.3041C>G (p.Thr1014Arg)
NM_020442.6(VARS2):c.304C>T (p.Pro102Ser)
NM_020442.6(VARS2):c.3050C>A (p.Thr1017Asn)
NM_020442.6(VARS2):c.3170C>A (p.Ala1057Asp)
NM_020442.6(VARS2):c.344C>G (p.Pro115Arg)
NM_020442.6(VARS2):c.413C>A (p.Thr138Asn)
NM_020442.6(VARS2):c.469G>A (p.Ala157Thr)
NM_020442.6(VARS2):c.604C>T (p.Arg202Trp)
NM_020442.6(VARS2):c.800C>T (p.Ala267Val)
NM_020442.6(VARS2):c.815G>A (p.Arg272Gln)
NM_020442.6(VARS2):c.859A>G (p.Ile287Val)
NM_020442.6(VARS2):c.869T>C (p.Ile290Thr)
NM_020442.6(VARS2):c.883C>T (p.Arg295Trp)

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