ClinVar Miner

List of variants studied for Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia by Illumina Clinical Services Laboratory,Illumina

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Total variants: 50
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HGVS dbSNP
NM_007126.3(VCP):c.-370G>A rs886063895
NM_007126.5(VCP):c.*1001C>T
NM_007126.5(VCP):c.*1040T>C
NM_007126.5(VCP):c.*12C>T
NM_007126.5(VCP):c.*153G>T rs1053318
NM_007126.5(VCP):c.*15C>T
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.*438A>G rs137953487
NM_007126.5(VCP):c.*4G>T rs201091341
NM_007126.5(VCP):c.*596C>T rs55745923
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.*906A>G rs76360394
NM_007126.5(VCP):c.-215A>G rs886063893
NM_007126.5(VCP):c.-250C>T rs886063894
NM_007126.5(VCP):c.-267C>T rs184152880
NM_007126.5(VCP):c.-53C>T rs369830702
NM_007126.5(VCP):c.1082-9G>T rs12349922
NM_007126.5(VCP):c.1092C>T (p.Asp364=) rs61752947
NM_007126.5(VCP):c.1293C>T (p.Asp431=)
NM_007126.5(VCP):c.130-9T>C
NM_007126.5(VCP):c.1360-14C>G rs144304208
NM_007126.5(VCP):c.1360-6T>C rs370296303
NM_007126.5(VCP):c.1584C>T (p.Ala528=) rs147623367
NM_007126.5(VCP):c.1695+8A>G rs684562
NM_007126.5(VCP):c.1704A>G (p.Gln568=) rs142577424
NM_007126.5(VCP):c.18-5T>C rs114256093
NM_007126.5(VCP):c.185A>G (p.Lys62Arg) rs886063892
NM_007126.5(VCP):c.2214A>G (p.Glu738=) rs374391034
NM_007126.5(VCP):c.2406T>C (p.Asp802=) rs145508640
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)
NM_007126.5(VCP):c.79A>G (p.Ile27Val) rs140913250
NM_007126.5(VCP):c.811+3G>A rs514492
NM_007126.5(VCP):c.812-7C>G
NM_007126.5(VCP):c.832T>C (p.Leu278=) rs200670526
NM_007126.5(VCP):c.927C>T (p.Ile309=) rs34097935

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