ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 46
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HGVS dbSNP
NM_001376.5(DYNC1H1):c.10380C>T (p.Ala3460=) rs1555411404
NM_001376.5(DYNC1H1):c.10548C>T (p.Tyr3516=) rs760532492
NM_001376.5(DYNC1H1):c.10832G>A (p.Arg3611Gln) rs760957660
NM_001376.5(DYNC1H1):c.11016G>A (p.Ser3672=) rs199679500
NM_001376.5(DYNC1H1):c.11045G>A (p.Arg3682Gln) rs1555411755
NM_001376.5(DYNC1H1):c.11245C>A (p.Leu3749Ile) rs1555411787
NM_001376.5(DYNC1H1):c.11520A>G (p.Leu3840=) rs369351359
NM_001376.5(DYNC1H1):c.11785G>A (p.Val3929Met) rs867293260
NM_001376.5(DYNC1H1):c.12181G>A (p.Glu4061Lys) rs797045530
NM_001376.5(DYNC1H1):c.12428G>A (p.Arg4143His) rs867634752
NM_001376.5(DYNC1H1):c.12759C>T (p.Gly4253=) rs529010293
NM_001376.5(DYNC1H1):c.13072G>A (p.Ala4358Thr) rs547205132
NM_001376.5(DYNC1H1):c.13261G>A (p.Ala4421Thr) rs376492799
NM_001376.5(DYNC1H1):c.13278C>T (p.Asp4426=) rs777098264
NM_001376.5(DYNC1H1):c.13440C>T (p.Ser4480=) rs150286673
NM_001376.5(DYNC1H1):c.2737G>A (p.Val913Ile) rs372740994
NM_001376.5(DYNC1H1):c.2971A>G (p.Met991Val) rs1057518524
NM_001376.5(DYNC1H1):c.3084T>G (p.Asp1028Glu) rs775528195
NM_001376.5(DYNC1H1):c.3156+5G>A rs200905961
NM_001376.5(DYNC1H1):c.3795G>T (p.Lys1265Asn) rs1555408996
NM_001376.5(DYNC1H1):c.3804G>A (p.Thr1268=) rs757595764
NM_001376.5(DYNC1H1):c.407G>A (p.Arg136Gln) rs996476189
NM_001376.5(DYNC1H1):c.4484A>G (p.Asn1495Ser) rs566164007
NM_001376.5(DYNC1H1):c.4515G>A (p.Ser1505=) rs186932188
NM_001376.5(DYNC1H1):c.4542+6G>A rs375822798
NM_001376.5(DYNC1H1):c.4580T>C (p.Leu1527Pro) rs879254213
NM_001376.5(DYNC1H1):c.5655T>A (p.Thr1885=) rs538791873
NM_001376.5(DYNC1H1):c.60C>G (p.Ala20=) rs1555407002
NM_001376.5(DYNC1H1):c.631C>G (p.Pro211Ala) rs1555407907
NM_001376.5(DYNC1H1):c.6468G>A (p.Leu2156=) rs797045531
NM_001376.5(DYNC1H1):c.6857+6T>G rs1555409996
NM_001376.5(DYNC1H1):c.6997C>T (p.Leu2333Phe) rs1131691358
NM_001376.5(DYNC1H1):c.7190G>A (p.Arg2397Gln) rs751820545
NM_001376.5(DYNC1H1):c.7192C>T (p.Arg2398Cys) rs141525226
NM_001376.5(DYNC1H1):c.751C>G (p.Arg251Gly) rs879253979
NM_001376.5(DYNC1H1):c.7746C>T (p.Tyr2582=) rs797045533
NM_001376.5(DYNC1H1):c.7758C>T (p.Ala2586=) rs145487328
NM_001376.5(DYNC1H1):c.7884A>G (p.Pro2628=) rs797045534
NM_001376.5(DYNC1H1):c.791G>A (p.Arg264Gln) rs713993043
NM_001376.5(DYNC1H1):c.8502A>G (p.Gln2834=) rs146220233
NM_001376.5(DYNC1H1):c.8876A>G (p.Tyr2959Cys) rs797045536
NM_001376.5(DYNC1H1):c.9138G>T (p.Ser3046=) rs34338935
NM_001376.5(DYNC1H1):c.9372T>C (p.Asp3124=) rs797045538
NM_001376.5(DYNC1H1):c.9403C>A (p.Gln3135Lys) rs1049866462
NM_001376.5(DYNC1H1):c.948_952del (p.Phe316_Asp317insTer) rs1555407963
NM_001376.5(DYNC1H1):c.9960G>T (p.Ala3320=) rs746026558

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