ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance for Spinocerebellar Ataxia, Dominant

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Total variants: 84
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HGVS dbSNP
NC_000014.9:g.101964570C>T
NM_001376.4(DYNC1H1):c.-137C>T rs886050367
NM_001376.5(DYNC1H1):c.*108G>A rs886050378
NM_001376.5(DYNC1H1):c.*194C>G
NM_001376.5(DYNC1H1):c.*70T>C
NM_001376.5(DYNC1H1):c.-90C>T
NM_001376.5(DYNC1H1):c.10320G>A (p.Leu3440=) rs886050371
NM_001376.5(DYNC1H1):c.10575T>C (p.Arg3525=) rs763119040
NM_001376.5(DYNC1H1):c.10752T>C (p.Asn3584=) rs181445947
NM_001376.5(DYNC1H1):c.10754+11G>A rs886050372
NM_001376.5(DYNC1H1):c.10800T>C (p.Ile3600=) rs886050373
NM_001376.5(DYNC1H1):c.10833G>C (p.Arg3611=) rs35143882
NM_001376.5(DYNC1H1):c.10843C>T (p.Leu3615=) rs886050374
NM_001376.5(DYNC1H1):c.10858A>G (p.Arg3620Gly)
NM_001376.5(DYNC1H1):c.1086A>G (p.Thr362=)
NM_001376.5(DYNC1H1):c.10896C>A (p.Pro3632=) rs200903643
NM_001376.5(DYNC1H1):c.11056-10A>G rs751676054
NM_001376.5(DYNC1H1):c.11132A>G (p.Gln3711Arg) rs886050375
NM_001376.5(DYNC1H1):c.11366T>C (p.Ile3789Thr)
NM_001376.5(DYNC1H1):c.11460+4G>A rs201518717
NM_001376.5(DYNC1H1):c.1158A>G (p.Arg386=)
NM_001376.5(DYNC1H1):c.11609G>A (p.Arg3870Gln)
NM_001376.5(DYNC1H1):c.11873G>T (p.Gly3958Val)
NM_001376.5(DYNC1H1):c.11898G>A (p.Pro3966=)
NM_001376.5(DYNC1H1):c.11913C>G (p.Pro3971=) rs201174299
NM_001376.5(DYNC1H1):c.12102+6G>A rs377669980
NM_001376.5(DYNC1H1):c.12453A>T (p.Pro4151=) rs200375220
NM_001376.5(DYNC1H1):c.12705G>A (p.Pro4235=) rs199792795
NM_001376.5(DYNC1H1):c.12887T>C (p.Met4296Thr) rs886050376
NM_001376.5(DYNC1H1):c.1296A>G (p.Val432=) rs767564445
NM_001376.5(DYNC1H1):c.13157A>G (p.Asn4386Ser) rs201575292
NM_001376.5(DYNC1H1):c.13350G>A (p.Thr4450=)
NM_001376.5(DYNC1H1):c.13515+8C>T rs200901713
NM_001376.5(DYNC1H1):c.13682C>T (p.Thr4561Met)
NM_001376.5(DYNC1H1):c.13707G>C (p.Thr4569=) rs138571942
NM_001376.5(DYNC1H1):c.13719C>T (p.Asn4573=) rs886050377
NM_001376.5(DYNC1H1):c.1560T>C (p.Ile520=) rs761916499
NM_001376.5(DYNC1H1):c.161C>T (p.Ala54Val) rs772070566
NM_001376.5(DYNC1H1):c.2328G>A (p.Pro776=) rs144921184
NM_001376.5(DYNC1H1):c.2352C>T (p.Ser784=)
NM_001376.5(DYNC1H1):c.2376C>T (p.Cys792=) rs35092963
NM_001376.5(DYNC1H1):c.2462C>T (p.Ala821Val)
NM_001376.5(DYNC1H1):c.249G>C (p.Thr83=)
NM_001376.5(DYNC1H1):c.2670G>T (p.Leu890=) rs142961295
NM_001376.5(DYNC1H1):c.2672A>G (p.His891Arg) rs774004189
NM_001376.5(DYNC1H1):c.2719-15T>C
NM_001376.5(DYNC1H1):c.2922A>C (p.Pro974=)
NM_001376.5(DYNC1H1):c.3033A>G (p.Glu1011=)
NM_001376.5(DYNC1H1):c.366T>C (p.Thr122=) rs527943422
NM_001376.5(DYNC1H1):c.3699G>T (p.Gln1233His)
NM_001376.5(DYNC1H1):c.390C>T (p.Pro130=)
NM_001376.5(DYNC1H1):c.4279T>C (p.Ser1427Pro)
NM_001376.5(DYNC1H1):c.4647T>G (p.Gly1549=)
NM_001376.5(DYNC1H1):c.4959C>T (p.His1653=) rs773425996
NM_001376.5(DYNC1H1):c.5049+15G>A
NM_001376.5(DYNC1H1):c.5050G>A (p.Val1684Ile) rs781664182
NM_001376.5(DYNC1H1):c.5217C>T (p.Ile1739=) rs886050368
NM_001376.5(DYNC1H1):c.5422C>A (p.Leu1808Ile) rs879253937
NM_001376.5(DYNC1H1):c.5424A>G (p.Leu1808=) rs770425304
NM_001376.5(DYNC1H1):c.5427A>G (p.Glu1809=)
NM_001376.5(DYNC1H1):c.5523G>A (p.Gln1841=)
NM_001376.5(DYNC1H1):c.579C>T (p.Leu193=)
NM_001376.5(DYNC1H1):c.5971G>A (p.Asp1991Asn) rs151001016
NM_001376.5(DYNC1H1):c.6030G>A (p.Pro2010=) rs202004938
NM_001376.5(DYNC1H1):c.6210C>G (p.Val2070=)
NM_001376.5(DYNC1H1):c.6339G>A (p.Arg2113=) rs776544497
NM_001376.5(DYNC1H1):c.6711G>A (p.Leu2237=) rs886050369
NM_001376.5(DYNC1H1):c.6883C>G (p.Leu2295Val)
NM_001376.5(DYNC1H1):c.6884T>G (p.Leu2295Arg)
NM_001376.5(DYNC1H1):c.7014+11T>A rs748466861
NM_001376.5(DYNC1H1):c.7077C>T (p.Cys2359=)
NM_001376.5(DYNC1H1):c.7127A>G (p.Asn2376Ser) rs775274723
NM_001376.5(DYNC1H1):c.7193G>A (p.Arg2398His) rs912429154
NM_001376.5(DYNC1H1):c.7431C>T (p.Pro2477=)
NM_001376.5(DYNC1H1):c.7442T>C (p.Met2481Thr)
NM_001376.5(DYNC1H1):c.8177+12C>T
NM_001376.5(DYNC1H1):c.8178-12A>T rs538986139
NM_001376.5(DYNC1H1):c.8808T>A (p.Ile2936=) rs886050370
NM_001376.5(DYNC1H1):c.9138G>A (p.Ser3046=)
NM_001376.5(DYNC1H1):c.9155A>G (p.Lys3052Arg)
NM_001376.5(DYNC1H1):c.9178C>T (p.Arg3060Cys) rs773658296
NM_001376.5(DYNC1H1):c.9210G>A (p.Pro3070=) rs201817995
NM_001376.5(DYNC1H1):c.9503C>T (p.Thr3168Met)
NM_001376.5(DYNC1H1):c.9531G>A (p.Leu3177=) rs531438720

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