ClinVar Miner

List of variants in gene LIAS reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_006859.4(LIAS):c.1029T>C (p.Thr343=)
NM_006859.4(LIAS):c.105A>G (p.Lys35=)
NM_006859.4(LIAS):c.1116C>G (p.Leu372=)
NM_006859.4(LIAS):c.114C>A (p.Leu38=) rs750439302
NM_006859.4(LIAS):c.114C>G (p.Leu38=)
NM_006859.4(LIAS):c.129A>G (p.Pro43=) rs377315137
NM_006859.4(LIAS):c.168G>A (p.Arg56=) rs768182597
NM_006859.4(LIAS):c.186T>C (p.Tyr62=) rs1166998501
NM_006859.4(LIAS):c.234A>G (p.Pro78=)
NM_006859.4(LIAS):c.297T>C (p.Asn99=) rs144299903
NM_006859.4(LIAS):c.330A>T (p.Arg110=)
NM_006859.4(LIAS):c.375C>T (p.Thr125=)
NM_006859.4(LIAS):c.387G>A (p.Thr129=) rs746196972
NM_006859.4(LIAS):c.393+7C>A rs372423537
NM_006859.4(LIAS):c.405C>T (p.Asp135=)
NM_006859.4(LIAS):c.45+7G>A
NM_006859.4(LIAS):c.46-5T>C
NM_006859.4(LIAS):c.529C>T (p.Leu177=) rs750168413
NM_006859.4(LIAS):c.550+9G>A
NM_006859.4(LIAS):c.60T>C (p.Tyr20=) rs201996792
NM_006859.4(LIAS):c.705A>C (p.Ala235=)
NM_006859.4(LIAS):c.723C>A (p.Val241=) rs1029290249
NM_006859.4(LIAS):c.737+10T>G
NM_006859.4(LIAS):c.737+9G>A rs750744754
NM_006859.4(LIAS):c.76A>G (p.Arg26Gly)
NM_006859.4(LIAS):c.807G>A (p.Gln269=) rs140846573
NM_006859.4(LIAS):c.81G>A (p.Pro27=) rs760501971
NM_006859.4(LIAS):c.884-4A>G
NM_006859.4(LIAS):c.884-5T>A rs374449188

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