ClinVar Miner

List of variants in gene VCP reported as likely benign 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: 13
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NM_007126.5(VCP):c.1017A>G (p.Ala339=) rs565534943
NM_007126.5(VCP):c.1202A>G (p.Asn401Ser) rs148329626
NM_007126.5(VCP):c.1329C>T (p.Asn443=) rs748816624
NM_007126.5(VCP):c.1696-7C>T rs1554668202
NM_007126.5(VCP):c.1950G>A (p.Glu650=) rs752382520
NM_007126.5(VCP):c.213C>T (p.Val71=) rs1195805928
NM_007126.5(VCP):c.2161-6C>T rs199513619
NM_007126.5(VCP):c.2316-4A>G rs755625059
NM_007126.5(VCP):c.2406T>C (p.Asp802=) rs145508640
NM_007126.5(VCP):c.2412G>A (p.Leu804=) rs757712897
NM_007126.5(VCP):c.426G>A (p.Ala142=) rs577812326
NM_007126.5(VCP):c.552C>T (p.Cys184=) rs769455914
NM_007126.5(VCP):c.576+10C>G rs757728490

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