ClinVar Miner

List of variants in gene PIGV reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_017837.4(PIGV):c.1200+205G>A rs146091102 0.02218
NM_017837.4(PIGV):c.-58+430G>A rs113210202 0.00790
NM_017837.4(PIGV):c.1277C>T (p.Pro426Leu) rs146969255 0.00109
NM_017837.4(PIGV):c.390T>C (p.Ala130=) rs139724134 0.00037
NM_017837.4(PIGV):c.879G>A (p.Pro293=) rs147229452 0.00031
NM_017837.4(PIGV):c.473G>A (p.Ser158Asn) rs201332799 0.00014
NM_017837.4(PIGV):c.1084A>C (p.Lys362Gln) rs376257064 0.00007
NM_017837.4(PIGV):c.1453C>T (p.Leu485=) rs751093917 0.00007
NM_017837.4(PIGV):c.115G>A (p.Glu39Lys) rs369275802 0.00005
NM_017837.4(PIGV):c.783C>T (p.Thr261=) rs141862926 0.00005
NM_017837.4(PIGV):c.804A>G (p.Ser268=) rs745595984 0.00005
NM_017837.4(PIGV):c.809G>A (p.Arg270His) rs149379900 0.00005
NM_017837.4(PIGV):c.258C>T (p.Ala86=) rs749928862 0.00003
NM_017837.4(PIGV):c.1278G>A (p.Pro426=) rs575831229 0.00002
NM_017837.4(PIGV):c.346C>T (p.Leu116=) rs149582139 0.00002
NM_017837.4(PIGV):c.450T>C (p.Tyr150=) rs765065261 0.00002
NM_017837.4(PIGV):c.876A>G (p.Glu292=) rs756422269 0.00002
NM_017837.4(PIGV):c.999A>C (p.Pro333=) rs764422244 0.00002
NM_017837.4(PIGV):c.-62C>T rs1229317654 0.00001
NM_017837.4(PIGV):c.1227C>T (p.Ser409=) rs756021930 0.00001
NM_017837.4(PIGV):c.183C>T (p.Gly61=) rs769117896 0.00001
NM_017837.4(PIGV):c.600T>C (p.Thr200=) rs946539785 0.00001
NM_017837.4(PIGV):c.735G>A (p.Val245=) rs762221948 0.00001
NM_017837.4(PIGV):c.111T>C (p.His37=) rs1057523852
NM_017837.4(PIGV):c.1155C>T (p.His385=) rs200817594
NM_017837.4(PIGV):c.1452C>G (p.Leu484=) rs148409472
NM_017837.4(PIGV):c.304T>C (p.Leu102=) rs2124193880
NM_017837.4(PIGV):c.333A>G (p.Leu111=) rs1186562909
NM_017837.4(PIGV):c.348_349delinsAG (p.Ile117Val) rs886044116
NM_017837.4(PIGV):c.354G>A (p.Ser118=) rs765982367
NM_017837.4(PIGV):c.354G>C (p.Ser118=) rs765982367
NM_017837.4(PIGV):c.684G>A (p.Leu228=) rs551364712
NM_017837.4(PIGV):c.945C>T (p.Gly315=) rs1553155059

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