ClinVar Miner

List of variants in gene combination IDS, LOC106050102 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: 44
Download table as spreadsheet
HGVS dbSNP
NM_000202.8(IDS):c.1006+8T>C rs782781942
NM_000202.8(IDS):c.1007-4C>T
NM_000202.8(IDS):c.1007-9A>G
NM_000202.8(IDS):c.1047C>T (p.Ser349=)
NM_000202.8(IDS):c.1085A>G (p.Tyr362Cys)
NM_000202.8(IDS):c.1100C>T (p.Thr367Met)
NM_000202.8(IDS):c.1112C>T (p.Pro371Leu) rs782471629
NM_000202.8(IDS):c.1113G>T (p.Pro371=) rs146615651
NM_000202.8(IDS):c.1122C>A (p.Gly374=)
NM_000202.8(IDS):c.1164A>G (p.Ser388=)
NM_000202.8(IDS):c.1180+7A>C
NM_000202.8(IDS):c.419-10T>G rs782082376
NM_000202.8(IDS):c.419-6T>C
NM_000202.8(IDS):c.450G>A (p.Pro150=) rs201892132
NM_000202.8(IDS):c.450G>T (p.Pro150=)
NM_000202.8(IDS):c.465T>C (p.Phe155=)
NM_000202.8(IDS):c.477T>C (p.His159=)
NM_000202.8(IDS):c.480T>A (p.Pro160=)
NM_000202.8(IDS):c.504T>A (p.Thr168=)
NM_000202.8(IDS):c.507+6G>T rs370769925
NM_000202.8(IDS):c.507+7C>T
NM_000202.8(IDS):c.508-5G>T
NM_000202.8(IDS):c.534C>T (p.Leu178=)
NM_000202.8(IDS):c.540C>T (p.Ala180=)
NM_000202.8(IDS):c.576C>T (p.Pro192=)
NM_000202.8(IDS):c.641C>T (p.Thr214Met) rs61736892
NM_000202.8(IDS):c.642G>A (p.Thr214=)
NM_000202.8(IDS):c.669T>G (p.Val223=)
NM_000202.8(IDS):c.693C>T (p.Pro231=)
NM_000202.8(IDS):c.696C>T (p.Phe232=) rs782498858
NM_000202.8(IDS):c.717G>A (p.Gln239=)
NM_000202.8(IDS):c.759C>G (p.Pro253=)
NM_000202.8(IDS):c.760G>A (p.Glu254Lys) rs374066256
NM_000202.8(IDS):c.777A>T (p.Leu259=) rs782773319
NM_000202.8(IDS):c.807C>T (p.Asp269=)
NM_000202.8(IDS):c.852G>A (p.Pro284=)
NM_000202.8(IDS):c.879+10A>G
NM_000202.8(IDS):c.880-5del
NM_000202.8(IDS):c.889C>T (p.Arg297Cys)
NM_000202.8(IDS):c.918T>C (p.Tyr306=)
NM_000202.8(IDS):c.929A>G (p.Gln310Arg)
NM_000202.8(IDS):c.933C>T (p.Val311=)
NM_000202.8(IDS):c.955G>A (p.Asp319Asn)
NM_000202.8(IDS):c.982A>G (p.Ile328Val)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.