ClinVar Miner

List of variants reported as uncertain significance for Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia

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Total variants: 28
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HGVS dbSNP
NM_007126.3(VCP):c.-370G>A rs886063895
NM_007126.5(VCP):c.*1040T>C
NM_007126.5(VCP):c.*172C>G rs886063890
NM_007126.5(VCP):c.*184G>A rs886063889
NM_007126.5(VCP):c.*216G>A
NM_007126.5(VCP):c.*217G>T
NM_007126.5(VCP):c.*347C>T rs886063888
NM_007126.5(VCP):c.*367G>A
NM_007126.5(VCP):c.*382C>T rs749381324
NM_007126.5(VCP):c.*63G>A
NM_007126.5(VCP):c.*64C>T rs553370942
NM_007126.5(VCP):c.*700C>A rs537730311
NM_007126.5(VCP):c.*788G>A rs886063887
NM_007126.5(VCP):c.*885G>A
NM_007126.5(VCP):c.-215A>G rs886063893
NM_007126.5(VCP):c.-250C>T rs886063894
NM_007126.5(VCP):c.-53C>T rs369830702
NM_007126.5(VCP):c.1293C>T (p.Asp431=)
NM_007126.5(VCP):c.130-9T>C
NM_007126.5(VCP):c.1360-6T>C rs370296303
NM_007126.5(VCP):c.1374G>C (p.Gln458His) rs1060499674
NM_007126.5(VCP):c.185A>G (p.Lys62Arg) rs886063892
NM_007126.5(VCP):c.335A>G (p.Lys112Arg)
NM_007126.5(VCP):c.384T>C (p.Gly128=)
NM_007126.5(VCP):c.446-4G>A
NM_007126.5(VCP):c.591C>G (p.Ser197=)
NM_007126.5(VCP):c.697A>G (p.Ile233Val)
NM_007126.5(VCP):c.794T>C (p.Phe265Ser)

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