ClinVar Miner

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

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Gene type:
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Total variants: 99
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HGVS dbSNP
NM_001376.5(DYNC1H1):c.10084G>A (p.Ala3362Thr) rs113879661
NM_001376.5(DYNC1H1):c.10346A>C (p.Glu3449Ala) rs1555411398
NM_001376.5(DYNC1H1):c.10354G>A (p.Ala3452Thr) rs1555411400
NM_001376.5(DYNC1H1):c.10656C>T (p.Tyr3552=) rs587780329
NM_001376.5(DYNC1H1):c.10682G>A (p.Arg3561His) rs1064796932
NM_001376.5(DYNC1H1):c.10743A>C (p.Lys3581Asn) rs768668529
NM_001376.5(DYNC1H1):c.10887C>T (p.Phe3629=) rs141133453
NM_001376.5(DYNC1H1):c.11086G>T (p.Val3696Phe) rs1555411772
NM_001376.5(DYNC1H1):c.11558C>G (p.Thr3853Arg) rs1567021411
NM_001376.5(DYNC1H1):c.11776G>C (p.Gly3926Arg) rs879254035
NM_001376.5(DYNC1H1):c.11863G>A (p.Glu3955Lys) rs767837334
NM_001376.5(DYNC1H1):c.11906C>A (p.Thr3969Asn) rs770525695
NM_001376.5(DYNC1H1):c.11995G>A (p.Asp3999Asn) rs879254105
NM_001376.5(DYNC1H1):c.12071C>T (p.Pro4024Leu) rs879254308
NM_001376.5(DYNC1H1):c.12450G>A (p.Pro4150=) rs749647281
NM_001376.5(DYNC1H1):c.12589G>A (p.Ala4197Thr) rs879254018
NM_001376.5(DYNC1H1):c.1276G>A (p.Glu426Lys) rs879254303
NM_001376.5(DYNC1H1):c.12853G>T (p.Ala4285Ser) rs749486351
NM_001376.5(DYNC1H1):c.12867C>T (p.Asp4289=) rs571858561
NM_001376.5(DYNC1H1):c.1288del (p.Leu430fs) rs1555408161
NM_001376.5(DYNC1H1):c.12905G>A (p.Arg4302Gln) rs755680664
NM_001376.5(DYNC1H1):c.13042A>C (p.Met4348Leu) rs879254327
NM_001376.5(DYNC1H1):c.1312G>A (p.Val438Ile) rs1034508175
NM_001376.5(DYNC1H1):c.13196A>G (p.Lys4399Arg) rs879253906
NM_001376.5(DYNC1H1):c.13199G>A (p.Arg4400His) rs879254217
NM_001376.5(DYNC1H1):c.13261G>A (p.Ala4421Thr) rs376492799
NM_001376.5(DYNC1H1):c.13286A>G (p.Gln4429Arg) rs763724110
NM_001376.5(DYNC1H1):c.13315G>A (p.Glu4439Lys) rs142883042
NM_001376.5(DYNC1H1):c.13349C>T (p.Thr4450Met) rs146087540
NM_001376.5(DYNC1H1):c.13360G>A (p.Glu4454Lys) rs1064797194
NM_001376.5(DYNC1H1):c.13384C>T (p.Arg4462Trp) rs879253914
NM_001376.5(DYNC1H1):c.13385G>A (p.Arg4462Gln) rs376608392
NM_001376.5(DYNC1H1):c.13509G>T (p.Glu4503Asp) rs1304570979
NM_001376.5(DYNC1H1):c.13557G>A (p.Ala4519=) rs35546990
NM_001376.5(DYNC1H1):c.13667G>A (p.Cys4556Tyr) rs142519155
NM_001376.5(DYNC1H1):c.13855A>G (p.Ile4619Val) rs879254286
NM_001376.5(DYNC1H1):c.1454G>A (p.Arg485Lys) rs879254275
NM_001376.5(DYNC1H1):c.1626C>T (p.Gly542=) rs1566998995
NM_001376.5(DYNC1H1):c.1887G>T (p.Gln629His) rs777262223
NM_001376.5(DYNC1H1):c.2147G>A (p.Arg716His) rs759802064
NM_001376.5(DYNC1H1):c.2155A>G (p.Thr719Ala) rs1064796870
NM_001376.5(DYNC1H1):c.2393G>A (p.Arg798Gln) rs768932305
NM_001376.5(DYNC1H1):c.294C>A (p.Phe98Leu) rs1064795200
NM_001376.5(DYNC1H1):c.3121A>G (p.Met1041Val) rs867890249
NM_001376.5(DYNC1H1):c.3156+5G>A rs200905961
NM_001376.5(DYNC1H1):c.3533G>A (p.Arg1178Gln) rs1057524432
NM_001376.5(DYNC1H1):c.3571C>T (p.Arg1191Cys) rs774198261
NM_001376.5(DYNC1H1):c.3704A>G (p.Gln1235Arg) rs867503066
NM_001376.5(DYNC1H1):c.3781T>C (p.Trp1261Arg) rs879253961
NM_001376.5(DYNC1H1):c.3803C>T (p.Thr1268Met) rs751865408
NM_001376.5(DYNC1H1):c.3804G>A (p.Thr1268=) rs757595764
NM_001376.5(DYNC1H1):c.4049C>T (p.Pro1350Leu) rs1131691955
NM_001376.5(DYNC1H1):c.4075-5G>A rs750127672
NM_001376.5(DYNC1H1):c.4510G>A (p.Val1504Ile) rs761695197
NM_001376.5(DYNC1H1):c.4624A>G (p.Arg1542Gly) rs1567006939
NM_001376.5(DYNC1H1):c.5074A>G (p.Ile1692Val) rs775895683
NM_001376.5(DYNC1H1):c.5209A>G (p.Thr1737Ala) rs1064797192
NM_001376.5(DYNC1H1):c.5294C>T (p.Ala1765Val) rs150687712
NM_001376.5(DYNC1H1):c.5347A>G (p.Ser1783Gly) rs773630385
NM_001376.5(DYNC1H1):c.5422C>A (p.Leu1808Ile) rs879253937
NM_001376.5(DYNC1H1):c.5589T>C (p.Asn1863=) rs1567008458
NM_001376.5(DYNC1H1):c.5818-4C>T rs532720319
NM_001376.5(DYNC1H1):c.6421G>A (p.Val2141Ile) rs765613848
NM_001376.5(DYNC1H1):c.6595G>C (p.Val2199Leu) rs1057524545
NM_001376.5(DYNC1H1):c.6739G>A (p.Val2247Met) rs1064796963
NM_001376.5(DYNC1H1):c.7127A>G (p.Asn2376Ser) rs775274723
NM_001376.5(DYNC1H1):c.7138G>A (p.Ala2380Thr) rs550161377
NM_001376.5(DYNC1H1):c.7192C>T (p.Arg2398Cys) rs141525226
NM_001376.5(DYNC1H1):c.7224C>T (p.Ala2408=) rs587780330
NM_001376.5(DYNC1H1):c.7403A>T (p.Asn2468Ile) rs797045532
NM_001376.5(DYNC1H1):c.7420G>A (p.Ala2474Thr) rs766837403
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.7544G>A (p.Gly2515Asp) rs1064797193
NM_001376.5(DYNC1H1):c.7565C>T (p.Thr2522Met) rs528647293
NM_001376.5(DYNC1H1):c.7570G>A (p.Val2524Met) rs147836678
NM_001376.5(DYNC1H1):c.7702G>T (p.Val2568Phe) rs765245789
NM_001376.5(DYNC1H1):c.7743G>T (p.Leu2581Phe) rs1236685924
NM_001376.5(DYNC1H1):c.791G>A (p.Arg264Gln) rs713993043
NM_001376.5(DYNC1H1):c.8097A>G (p.Thr2699=) rs772002773
NM_001376.5(DYNC1H1):c.8186G>A (p.Arg2729His) rs1000550855
NM_001376.5(DYNC1H1):c.8255A>G (p.Asn2752Ser) rs879253915
NM_001376.5(DYNC1H1):c.8275A>G (p.Ile2759Val) rs1131691452
NM_001376.5(DYNC1H1):c.8416A>G (p.Ile2806Val) rs777184216
NM_001376.5(DYNC1H1):c.8432G>T (p.Arg2811Ile) rs774929269
NM_001376.5(DYNC1H1):c.8442G>C (p.Glu2814Asp) rs762494017
NM_001376.5(DYNC1H1):c.8478A>G (p.Ala2826=) rs117846737
NM_001376.5(DYNC1H1):c.8703T>C (p.Tyr2901=) rs755411424
NM_001376.5(DYNC1H1):c.8771+4G>A rs1555410867
NM_001376.5(DYNC1H1):c.8843G>A (p.Arg2948His) rs780690762
NM_001376.5(DYNC1H1):c.8954G>C (p.Cys2985Ser) rs1269870036
NM_001376.5(DYNC1H1):c.9049G>A (p.Val3017Met) rs879254170
NM_001376.5(DYNC1H1):c.9069A>G (p.Gly3023=) rs532073330
NM_001376.5(DYNC1H1):c.9142G>A (p.Glu3048Lys) rs1555410941
NM_001376.5(DYNC1H1):c.9178C>T (p.Arg3060Cys) rs773658296
NM_001376.5(DYNC1H1):c.9242C>T (p.Thr3081Ile) rs1555410958
NM_001376.5(DYNC1H1):c.9333T>A (p.Ser3111Arg) rs879254260
NM_001376.5(DYNC1H1):c.9642+13C>T rs760557941
NM_001376.5(DYNC1H1):c.9655C>T (p.Arg3219Cys) rs1555411141

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