ClinVar Miner

List of variants in gene DYNC2H1 reported as likely benign for not specified

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_001377.3(DYNC2H1):c.10864C>A (p.Arg3622=) rs117178504 0.00672
NM_001377.3(DYNC2H1):c.11726-10A>T rs185916947 0.00561
NM_001377.3(DYNC2H1):c.6477+14A>T rs111970770 0.00460
NM_001377.3(DYNC2H1):c.1263C>A (p.Phe421Leu) rs142881106 0.00365
NM_001377.3(DYNC2H1):c.10650A>G (p.Ser3550=) rs185562630 0.00361
NM_001377.3(DYNC2H1):c.9939T>C (p.Ala3313=) rs192003811 0.00327
NM_001377.3(DYNC2H1):c.8881G>A (p.Ala2961Thr) rs199568537 0.00317
NM_001377.3(DYNC2H1):c.1484A>C (p.Lys495Thr) rs202233363 0.00255
NM_001377.3(DYNC2H1):c.9814T>A (p.Leu3272Ile) rs200342335 0.00236
NM_001377.3(DYNC2H1):c.6909C>T (p.Tyr2303=) rs191012679 0.00210
NM_001377.3(DYNC2H1):c.7128A>G (p.Ala2376=) rs371410128 0.00193
NM_001377.3(DYNC2H1):c.3682C>A (p.Leu1228Ile) rs189806840 0.00189
NM_001377.3(DYNC2H1):c.10314A>G (p.Glu3438=) rs369838929 0.00188
NM_001377.3(DYNC2H1):c.5047C>T (p.Leu1683Phe) rs201563576 0.00172
NM_001377.3(DYNC2H1):c.12366+8A>G rs200404815 0.00156
NM_001377.3(DYNC2H1):c.9749A>G (p.Gln3250Arg) rs140830294 0.00151
NM_001377.3(DYNC2H1):c.3015A>G (p.Leu1005=) rs201310509 0.00128
NM_001377.3(DYNC2H1):c.12566+17A>G rs187787132 0.00113
NM_001377.3(DYNC2H1):c.6918A>G (p.Ser2306=) rs368824340 0.00102
NM_001377.3(DYNC2H1):c.3744+9C>T rs142483417 0.00101
NM_001377.3(DYNC2H1):c.6551A>T (p.Asp2184Val) rs201967064 0.00101
NM_001377.3(DYNC2H1):c.9505A>G (p.Ile3169Val) rs200170585 0.00090
NM_001377.3(DYNC2H1):c.1135-11_1135-8del rs551487728 0.00064
NM_001377.3(DYNC2H1):c.5449A>G (p.Met1817Val) rs200208000 0.00064
NM_001377.3(DYNC2H1):c.7708+9A>G rs375081757 0.00063
NM_001377.3(DYNC2H1):c.11022+7T>A rs190701725 0.00062
NM_001377.3(DYNC2H1):c.12039+15A>G rs184350782 0.00059
NM_001377.3(DYNC2H1):c.2244C>T (p.His748=) rs373707570 0.00039
NM_001377.3(DYNC2H1):c.3735C>T (p.Ala1245=) rs377584612 0.00021
NM_001377.3(DYNC2H1):c.12039+19C>T rs778374973 0.00017
NM_001377.3(DYNC2H1):c.9231+12G>A rs369045696 0.00012
NM_001377.3(DYNC2H1):c.6057A>G (p.Leu2019=) rs187190605 0.00011
NM_001377.3(DYNC2H1):c.348C>T (p.Phe116=) rs776765795 0.00002
NM_001377.3(DYNC2H1):c.503-18C>G rs199660214 0.00002
NM_001377.3(DYNC2H1):c.12622C>T (p.Leu4208=) rs752163457 0.00001
NM_001377.3(DYNC2H1):c.5673T>C (p.Asn1891=) rs1197246634 0.00001
NM_001377.3(DYNC2H1):c.8946+10A>C rs550521675 0.00001
NM_001377.3(DYNC2H1):c.-40C>T rs1555034658
NM_001377.3(DYNC2H1):c.10043-7dup rs571044263
NM_001377.3(DYNC2H1):c.10980G>A (p.Glu3660=) rs1555090192
NM_001377.3(DYNC2H1):c.11096-17T>A rs1555095203
NM_001377.3(DYNC2H1):c.11096-9A>G
NM_001377.3(DYNC2H1):c.11650-16_11650-15dup rs760869137
NM_001377.3(DYNC2H1):c.12366+7_12366+8delinsAG rs1555119964
NM_001377.3(DYNC2H1):c.12672A>T (p.Gly4224=) rs1224616008
NM_001377.3(DYNC2H1):c.1679G>A (p.Arg560Gln) rs561232842
NM_001377.3(DYNC2H1):c.5784A>G (p.Gly1928=) rs1555057066

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