ClinVar Miner

List of variants in gene VCP reported as uncertain significance for amyotrophic lateral sclerosis type 14

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_007126.5(VCP):c.1180G>A (p.Val394Met)
NM_007126.5(VCP):c.1194+3G>A
NM_007126.5(VCP):c.1327A>C (p.Asn443His) rs770514866
NM_007126.5(VCP):c.1360-4C>G rs769279961
NM_007126.5(VCP):c.1374G>C (p.Gln458His) rs1060499674
NM_007126.5(VCP):c.1984C>T (p.Arg662Cys)
NM_007126.5(VCP):c.2014T>G (p.Leu672Val)
NM_007126.5(VCP):c.2266G>A (p.Glu756Lys)
NM_007126.5(VCP):c.2397C>G (p.Asp799Glu) rs1329151473
NM_007126.5(VCP):c.278G>A (p.Arg93His) rs779959657
NM_007126.5(VCP):c.303-3C>T rs1183711292
NM_007126.5(VCP):c.320A>T (p.Asp107Val) rs1563980440
NM_007126.5(VCP):c.340A>G (p.Ile114Val)
NM_007126.5(VCP):c.374G>A (p.Gly125Asp) rs1563980403
NM_007126.5(VCP):c.463C>G (p.Arg155Gly) rs121909330
NM_007126.5(VCP):c.478G>C (p.Ala160Pro) rs1554668805
NM_007126.5(VCP):c.479C>T (p.Ala160Val) rs1554668804
NM_007126.5(VCP):c.512G>T (p.Ser171Ile)
NM_007126.5(VCP):c.553G>A (p.Glu185Lys) rs864309501
NM_007126.5(VCP):c.811+2_811+3inv rs1554668584
NM_007126.5(VCP):c.84T>A (p.Val28=)

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