ClinVar Miner

List of variants in gene IVNS1ABP reported by Ambry Genetics

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Gene type:
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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_006469.5(IVNS1ABP):c.654A>T (p.Glu218Asp) rs35346683 0.00021
NM_006469.5(IVNS1ABP):c.1278C>G (p.His426Gln) rs139263536 0.00016
NM_006469.5(IVNS1ABP):c.1490C>T (p.Pro497Leu) rs201979152 0.00015
NM_006469.5(IVNS1ABP):c.217G>A (p.Val73Ile) rs146352011 0.00012
NM_006469.5(IVNS1ABP):c.199C>A (p.Pro67Thr) rs202151175 0.00005
NM_006469.5(IVNS1ABP):c.236A>G (p.Asn79Ser) rs780169380 0.00003
NM_006469.5(IVNS1ABP):c.1423G>A (p.Gly475Ser) rs200137725 0.00002
NM_006469.5(IVNS1ABP):c.553A>C (p.Asn185His) rs767693160 0.00002
NM_006469.5(IVNS1ABP):c.1324G>T (p.Asp442Tyr) rs768138174 0.00001
NM_006469.5(IVNS1ABP):c.1402G>A (p.Val468Ile)
NM_006469.5(IVNS1ABP):c.1592G>A (p.Arg531Gln)
NM_006469.5(IVNS1ABP):c.1804G>T (p.Ala602Ser)
NM_006469.5(IVNS1ABP):c.1910C>T (p.Thr637Ile) rs750061329
NM_006469.5(IVNS1ABP):c.504G>C (p.Glu168Asp)
NM_006469.5(IVNS1ABP):c.560G>C (p.Cys187Ser)
NM_006469.5(IVNS1ABP):c.605T>G (p.Val202Gly) rs1665757644
NM_006469.5(IVNS1ABP):c.610C>T (p.Arg204Cys) rs745491726
NM_006469.5(IVNS1ABP):c.842C>G (p.Thr281Arg)

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