ClinVar Miner

List of variants in gene DCDC2 studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_016356.5(DCDC2):c.1017C>T (p.Val339=) rs9467075
NM_016356.5(DCDC2):c.1044C>T (p.Asp348=) rs143313706
NM_016356.5(DCDC2):c.1076A>T (p.Asp359Val)
NM_016356.5(DCDC2):c.1099T>A (p.Ser367Thr)
NM_016356.5(DCDC2):c.1154C>T (p.Pro385Leu) rs773020868
NM_016356.5(DCDC2):c.1199G>A (p.Arg400His) rs771591530
NM_016356.5(DCDC2):c.1208G>A (p.Arg403His) rs139858268
NM_016356.5(DCDC2):c.1271A>C (p.Gln424Pro) rs794729665
NM_016356.5(DCDC2):c.1368A>T (p.Lys456Asn) rs9460973
NM_016356.5(DCDC2):c.294-21GTTT[2] rs374485384
NM_016356.5(DCDC2):c.349-9C>G rs765613994
NM_016356.5(DCDC2):c.349G>A (p.Val117Ile)
NM_016356.5(DCDC2):c.355C>T (p.Pro119Ser) rs1056029060
NM_016356.5(DCDC2):c.454C>G (p.Pro152Ala) rs33914824
NM_016356.5(DCDC2):c.471T>G (p.Leu157=)
NM_016356.5(DCDC2):c.478A>C (p.Arg160=) rs201204772
NM_016356.5(DCDC2):c.529dup (p.Ile177fs) rs904944428
NM_016356.5(DCDC2):c.543C>A (p.Ser181Arg) rs141060456
NM_016356.5(DCDC2):c.543C>T (p.Ser181=) rs141060456
NM_016356.5(DCDC2):c.549dup (p.Val184fs) rs1581640646
NM_016356.5(DCDC2):c.661A>G (p.Ser221Gly) rs2274305
NM_016356.5(DCDC2):c.685A>G (p.Thr229Ala)
NM_016356.5(DCDC2):c.705-4A>C
NM_016356.5(DCDC2):c.715T>G (p.Ser239Ala) rs144695853
NM_016356.5(DCDC2):c.728C>G (p.Pro243Arg)
NM_016356.5(DCDC2):c.750T>G (p.Ser250=) rs372157851
NM_016356.5(DCDC2):c.785C>T (p.Thr262Ile) rs200534758
NM_016356.5(DCDC2):c.829A>T (p.Lys277Ter) rs775868003
NM_016356.5(DCDC2):c.855A>G (p.Ser285=) rs141519329
NM_016356.5(DCDC2):c.929G>C (p.Gly310Ala) rs746447569
NM_016356.5(DCDC2):c.970G>T (p.Ala324Ser)
NM_016356.5(DCDC2):c.970dup (p.Ala324fs) rs774115675

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