ClinVar Miner

List of variants reported as uncertain significance for atrial fibrillation, familial, 11 by Invitae

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NC_000001.10:g.(?_147230250)_(147231366_?)dup
NC_000001.10:g.(?_147230260)_(147245383_?)del
NC_000001.10:g.(?_147230260)_(147245383_?)dup
NM_181703.4(GJA5):c.1006G>A (p.Gly336Ser)
NM_181703.4(GJA5):c.1024C>T (p.Arg342Ter)
NM_181703.4(GJA5):c.1035_1038del (p.Ser345fs)
NM_181703.4(GJA5):c.148G>A (p.Ala50Thr) rs782167622
NM_181703.4(GJA5):c.170T>G (p.Ile57Ser)
NM_181703.4(GJA5):c.199G>A (p.Asp67Asn)
NM_181703.4(GJA5):c.199G>T (p.Asp67Tyr) rs150906806
NM_181703.4(GJA5):c.259A>T (p.Thr87Ser) rs1557943770
NM_181703.4(GJA5):c.278T>C (p.Met93Thr)
NM_181703.4(GJA5):c.286G>T (p.Ala96Ser) rs121434557
NM_181703.4(GJA5):c.297T>G (p.Thr99=)
NM_181703.4(GJA5):c.325C>T (p.Arg109Trp) rs782392307
NM_181703.4(GJA5):c.358T>C (p.Ser120Pro)
NM_181703.4(GJA5):c.365C>T (p.Ser122Phe) rs781831348
NM_181703.4(GJA5):c.411G>T (p.Glu137Asp) rs200288659
NM_181703.4(GJA5):c.430G>A (p.Ala144Thr) rs782438073
NM_181703.4(GJA5):c.433del (p.Leu145fs) rs781802553
NM_181703.4(GJA5):c.478C>T (p.Arg160Cys)
NM_181703.4(GJA5):c.479G>T (p.Arg160Leu)
NM_181703.4(GJA5):c.496G>A (p.Gly166Ser) rs782065420
NM_181703.4(GJA5):c.525C>G (p.Tyr175Ter)
NM_181703.4(GJA5):c.592G>A (p.Val198Ile)
NM_181703.4(GJA5):c.771dup (p.Val258fs)
NM_181703.4(GJA5):c.787C>T (p.Pro263Ser)
NM_181703.4(GJA5):c.790C>A (p.Pro264Thr)
NM_181703.4(GJA5):c.793C>T (p.Pro265Ser) rs148311482
NM_181703.4(GJA5):c.941A>G (p.Gln314Arg)
NM_181703.4(GJA5):c.947G>A (p.Arg316His)
NM_181703.4(GJA5):c.973A>C (p.Asn325His) rs782592443
NM_181703.4(GJA5):c.977G>A (p.Gly326Glu) rs782703462

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