ClinVar Miner

List of variants in gene KCNJ10 reported as pathogenic for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys) rs137853074
NM_002241.5(KCNJ10):c.193C>T (p.Arg65Cys) rs387906834
NM_002241.5(KCNJ10):c.194G>C (p.Arg65Pro) rs137853066
NM_002241.5(KCNJ10):c.225T>G (p.Phe75Leu) rs757159382
NM_002241.5(KCNJ10):c.229G>C (p.Gly77Arg) rs137853072
NM_002241.5(KCNJ10):c.321_322del (p.Val109fs)
NM_002241.5(KCNJ10):c.418T>C (p.Cys140Arg) rs137853068
NM_002241.5(KCNJ10):c.491C>T (p.Thr164Ile) rs137853069
NM_002241.5(KCNJ10):c.500C>T (p.Ala167Val) rs137853070
NM_002241.5(KCNJ10):c.524G>A (p.Arg175Gln) rs397514673
NM_002241.5(KCNJ10):c.581C>A (p.Pro194His) rs137853073
NM_002241.5(KCNJ10):c.595C>T (p.Arg199Ter) rs137853067
NM_002241.5(KCNJ10):c.76C>T (p.Arg26Ter) rs138943405
NM_002241.5(KCNJ10):c.775del (p.Val258_Val259insTer) rs1557967748
NM_002241.5(KCNJ10):c.889C>T (p.Arg297Cys) rs137853071

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