ClinVar Miner

List of variants in gene PDK3 studied for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NC_000023.10:g.(?_24483553)_(24483698_?)del
NC_000023.10:g.(?_24483553)_(24557301_?)dup
NC_000023.10:g.(?_24512839)_(24557301_?)del
NM_001142386.3(PDK3):c.1228A>C (p.Lys410Gln) rs141326782
NM_005391.4(PDK3):c.1083T>C (p.Leu361=) rs746261967
NM_005391.4(PDK3):c.1087dup (p.Ser363fs) rs1569228214
NM_005391.4(PDK3):c.1126G>A (p.Ala376Thr)
NM_005391.4(PDK3):c.160C>T (p.Pro54Ser) rs1569221445
NM_005391.4(PDK3):c.249-8C>T rs1231289510
NM_005391.4(PDK3):c.282T>C (p.Tyr94=) rs201198782
NM_005391.4(PDK3):c.320+6T>C rs748960946
NM_005391.4(PDK3):c.336G>C (p.Leu112=) rs372442017
NM_005391.4(PDK3):c.376A>G (p.Met126Val) rs138321172
NM_005391.4(PDK3):c.473G>A (p.Arg158His) rs397515323
NM_005391.4(PDK3):c.474C>T (p.Arg158=)
NM_005391.4(PDK3):c.486C>T (p.Arg162=)
NM_005391.4(PDK3):c.51G>C (p.Glu17Asp) rs371137355
NM_005391.4(PDK3):c.562G>A (p.Asp188Asn) rs1165981822
NM_005391.4(PDK3):c.582G>A (p.Ala194=)
NM_005391.4(PDK3):c.597del (p.Asp199fs) rs1569225940
NM_005391.4(PDK3):c.608C>G (p.Thr203Arg) rs1555949588
NM_005391.4(PDK3):c.751-10A>G rs372774822
NM_005391.4(PDK3):c.798C>A (p.Gly266=) rs1250656724
NM_005391.4(PDK3):c.811A>G (p.Lys271Glu)

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