ClinVar Miner

List of variants studied for auriculocondylar syndrome 1

Included ClinVar conditions (2):
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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001377142.1(PLCB4):c.*563del rs148015873 0.01013
NM_001377142.1(PLCB4):c.*469G>T rs886056986 0.00005
NM_001377142.1(PLCB4):c.1897C>T (p.Arg633Cys) rs397514482 0.00003
NM_001377142.1(PLCB4):c.*1585dup rs565091978
NM_001377142.1(PLCB4):c.*1672del rs886056991
NM_001377142.1(PLCB4):c.1898G>A (p.Arg633His) rs397514481
NM_001377142.1(PLCB4):c.1904A>G (p.Tyr635Cys) rs397514480
NM_001377142.1(PLCB4):c.1984A>C (p.Asn662His) rs397514483
NM_001377142.1(PLCB4):c.3409-4del rs886056984
NM_001377142.1(PLCB4):c.3496-5_3496-2del rs886056985
NM_001377142.1(PLCB4):c.986A>C (p.Asn329Thr) rs387907179
NM_006496.4(GNAI3):c.118G>C (p.Gly40Arg) rs387907178
NM_006496.4(GNAI3):c.136A>G (p.Lys46Glu)
NM_006496.4(GNAI3):c.140G>A (p.Ser47Asn) rs1553223897
NM_006496.4(GNAI3):c.141C>A (p.Ser47Arg) rs397514768
NM_006496.4(GNAI3):c.145A>G (p.Ile49Val)
NM_006496.4(GNAI3):c.146T>C (p.Ile49Thr) rs1553223899
NM_006496.4(GNAI3):c.303+1G>A rs1648676750

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