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
NM_001080463.1(DYNC2H1):c.-40C>T rs1555034658
NM_001080463.1(DYNC2H1):c.10064-7dup rs571044263
NM_001080463.1(DYNC2H1):c.10335A>G (p.Glu3445=) rs369838929
NM_001080463.1(DYNC2H1):c.10671A>G (p.Ser3557=) rs185562630
NM_001080463.1(DYNC2H1):c.10885C>A (p.Arg3629=) rs117178504
NM_001080463.1(DYNC2H1):c.11001G>A (p.Glu3667=) rs1555090192
NM_001080463.1(DYNC2H1):c.11043+7T>A rs190701725
NM_001080463.1(DYNC2H1):c.11117-17T>A rs1555095203
NM_001080463.1(DYNC2H1):c.1135-11_1135-8delAATG rs551487728
NM_001080463.1(DYNC2H1):c.11671-16_11671-15dup rs760869137
NM_001080463.1(DYNC2H1):c.11724C>T (p.Asn3908=) rs144624858
NM_001080463.1(DYNC2H1):c.11747-10A>T rs185916947
NM_001080463.1(DYNC2H1):c.12060+15A>G rs184350782
NM_001080463.1(DYNC2H1):c.12060+19C>T rs778374973
NM_001080463.1(DYNC2H1):c.12387+7_12387+8delGAinsAG rs1555119964
NM_001080463.1(DYNC2H1):c.12587+17A>G rs187787132
NM_001080463.1(DYNC2H1):c.12643C>T (p.Leu4215=) rs752163457
NM_001080463.1(DYNC2H1):c.12693A>T (p.Gly4231=) rs1224616008
NM_001080463.1(DYNC2H1):c.1484A>C (p.Lys495Thr) rs202233363
NM_001080463.1(DYNC2H1):c.1679G>A (p.Arg560Gln) rs561232842
NM_001080463.1(DYNC2H1):c.27G>T (p.Arg9=) rs113537035
NM_001080463.1(DYNC2H1):c.3015A>G (p.Leu1005=) rs201310509
NM_001080463.1(DYNC2H1):c.3181C>G (p.Leu1061Val) rs200466720
NM_001080463.1(DYNC2H1):c.348C>T (p.Phe116=) rs776765795
NM_001080463.1(DYNC2H1):c.3682C>A (p.Leu1228Ile) rs189806840
NM_001080463.1(DYNC2H1):c.3735C>T (p.Ala1245=) rs377584612
NM_001080463.1(DYNC2H1):c.3744+9C>T rs142483417
NM_001080463.1(DYNC2H1):c.4312T>C (p.Leu1438=) rs367841359
NM_001080463.1(DYNC2H1):c.503-18C>G rs199660214
NM_001080463.1(DYNC2H1):c.5047C>T (p.Leu1683Phe) rs201563576
NM_001080463.1(DYNC2H1):c.5449A>G (p.Met1817Val) rs200208000
NM_001080463.1(DYNC2H1):c.5673T>C (p.Asn1891=) rs1197246634
NM_001080463.1(DYNC2H1):c.5784A>G (p.Gly1928=) rs1555057066
NM_001080463.1(DYNC2H1):c.6057A>G (p.Leu2019=) rs187190605
NM_001080463.1(DYNC2H1):c.6477+14A>T rs111970770
NM_001080463.1(DYNC2H1):c.6551A>T (p.Asp2184Val) rs201967064
NM_001080463.1(DYNC2H1):c.6894-4G>A rs17100043
NM_001080463.1(DYNC2H1):c.6909C>T (p.Tyr2303=) rs191012679
NM_001080463.1(DYNC2H1):c.6918A>G (p.Ser2306=) rs368824340
NM_001080463.1(DYNC2H1):c.7128A>G (p.Ala2376=) rs371410128
NM_001080463.1(DYNC2H1):c.7708+9A>G rs375081757
NM_001080463.1(DYNC2H1):c.8481A>C (p.Thr2827=) rs370627443
NM_001080463.1(DYNC2H1):c.8881G>A (p.Ala2961Thr) rs199568537
NM_001080463.1(DYNC2H1):c.9231+12G>A rs369045696
NM_001080463.1(DYNC2H1):c.9814T>A (p.Leu3272Ile) rs200342335
NM_001080463.1(DYNC2H1):c.9886G>C (p.Glu3296Gln) rs200326353
NM_001080463.1(DYNC2H1):c.9960T>C (p.Ala3320=) rs192003811

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