ClinVar Miner

List of variants in gene DYNC1H1 reported as likely pathogenic

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Gene type:
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Total variants: 42
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HGVS dbSNP
NC_000014.9:g.101979787T>G
NM_001376.5(DYNC1H1):c.10051A>T (p.Ile3351Phe) rs1567018763
NM_001376.5(DYNC1H1):c.1013A>G (p.Asp338Gly) rs879254267
NM_001376.5(DYNC1H1):c.1013A>T (p.Asp338Val) rs879254267
NM_001376.5(DYNC1H1):c.10160T>C (p.Leu3387Pro) rs1567019064
NM_001376.5(DYNC1H1):c.10172C>T (p.Pro3391Leu) rs1555411378
NM_001376.5(DYNC1H1):c.10280A>C (p.Gln3427Pro) rs1555411394
NM_001376.5(DYNC1H1):c.11183G>C (p.Arg3728Pro) rs797045529
NM_001376.5(DYNC1H1):c.11897C>G (p.Pro3966Arg) rs879254021
NM_001376.5(DYNC1H1):c.1700G>A (p.Arg567His) rs587781253
NM_001376.5(DYNC1H1):c.1702C>A (p.Leu568Ile) rs1057523839
NM_001376.5(DYNC1H1):c.1741A>T (p.Met581Leu) rs1566999047
NM_001376.5(DYNC1H1):c.1792C>T (p.Arg598Cys) rs587780564
NM_001376.5(DYNC1H1):c.1793G>A (p.Arg598His) rs879254085
NM_001376.5(DYNC1H1):c.1793G>T (p.Arg598Leu) rs879254085
NM_001376.5(DYNC1H1):c.1802T>A (p.Ile601Asn) rs1057518776
NM_001376.5(DYNC1H1):c.1827C>G (p.Ile609Met) rs760971556
NM_001376.5(DYNC1H1):c.1869C>G (p.Phe623Leu) rs1057518250
NM_001376.5(DYNC1H1):c.256+5G>C rs879254284
NM_001376.5(DYNC1H1):c.3980A>C (p.Gln1327Pro) rs763711252
NM_001376.5(DYNC1H1):c.4042G>A (p.Glu1348Lys) rs1047509819
NM_001376.5(DYNC1H1):c.4235A>G (p.His1412Arg) rs1064795677
NM_001376.5(DYNC1H1):c.4700G>T (p.Arg1567Leu) rs797044901
NM_001376.5(DYNC1H1):c.4741A>G (p.Lys1581Glu) rs879254112
NM_001376.5(DYNC1H1):c.4868G>A (p.Arg1623Gln) rs1064796765
NM_001376.5(DYNC1H1):c.5885G>A (p.Arg1962His) rs1057518287
NM_001376.5(DYNC1H1):c.6122T>C (p.Met2041Thr) rs1555409836
NM_001376.5(DYNC1H1):c.6260A>G (p.Asp2087Gly) rs1555409850
NM_001376.5(DYNC1H1):c.6271C>T (p.Arg2091Trp) rs866242352
NM_001376.5(DYNC1H1):c.6490G>A (p.Val2164Met) rs1567010427
NM_001376.5(DYNC1H1):c.6989G>A (p.Gly2330Glu) rs1555410010
NM_001376.5(DYNC1H1):c.6994C>T (p.Arg2332Cys) rs1057518961
NM_001376.5(DYNC1H1):c.7064C>T (p.Thr2355Ile) rs1555410129
NM_001376.5(DYNC1H1):c.7072C>T (p.Arg2358Cys) rs879254019
NM_001376.5(DYNC1H1):c.751C>T (p.Arg251Cys) rs879253979
NM_001376.5(DYNC1H1):c.752G>A (p.Arg251His) rs794727634
NM_001376.5(DYNC1H1):c.7793G>T (p.Gly2598Val) rs879253971
NM_001376.5(DYNC1H1):c.7918G>A (p.Glu2640Lys) rs797045535
NM_001376.5(DYNC1H1):c.829T>G (p.Phe277Val) rs1057518935
NM_001376.5(DYNC1H1):c.926G>A (p.Arg309His) rs797045177
NM_001376.5(DYNC1H1):c.9684G>C (p.Glu3228Asp) rs1555411143
NM_001376.5(DYNC1H1):c.9959C>T (p.Ala3320Val) rs1555411305

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