ClinVar Miner

List of variants in gene CHST14 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_130468.3(CHST14):c.1081C>G (p.Leu361Val) rs1566969372
NM_130468.3(CHST14):c.130A>G (p.Met44Val) rs1043447552
NM_130468.3(CHST14):c.148A>T (p.Ile50Phe) rs1046833753
NM_130468.3(CHST14):c.158C>A (p.Ser53Tyr)
NM_130468.3(CHST14):c.250C>A (p.Arg84Ser)
NM_130468.3(CHST14):c.275G>T (p.Gly92Val) rs754720949
NM_130468.3(CHST14):c.468G>C (p.Lys156Asn) rs1555410748
NM_130468.3(CHST14):c.548A>G (p.Asp183Gly)
NM_130468.3(CHST14):c.77C>T (p.Pro26Leu)
NM_130468.3(CHST14):c.869C>T (p.Ala290Val) rs763074027
NM_130468.4(CHST14):c.436C>G (p.Arg146Gly)

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