ClinVar Miner

List of variants in gene combination IDS, LOC106050102 reported as benign for Mucopolysaccharidosis, MPS-II

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_000202.8(IDS):c.438C>T (p.Thr146=) rs1141608 0.32051
NM_000202.8(IDS):c.641C>T (p.Thr214Met) rs61736892 0.01492
NM_000202.8(IDS):c.467C>A (p.Pro156Gln) rs145231211 0.00832
NM_000202.8(IDS):c.465T>A (p.Phe155Leu) rs149210251 0.00829
NM_000202.8(IDS):c.925A>G (p.Thr309Ala) rs145807417 0.00488
NM_000202.8(IDS):c.754G>A (p.Asp252Asn) rs146458524 0.00372
NM_000202.8(IDS):c.825C>T (p.Asp275=) rs148038243 0.00120
NM_000202.8(IDS):c.884A>G (p.Lys295Arg) rs113993953 0.00072
NM_000202.8(IDS):c.781C>G (p.Pro261Ala) rs141720810 0.00055
NM_000202.8(IDS):c.666C>T (p.Ala222=) rs201588028 0.00036
NM_000202.8(IDS):c.1074C>G (p.Pro358=) rs61736891 0.00035
NM_000202.8(IDS):c.727C>T (p.Pro243Ser) rs143474305 0.00023
NM_000202.8(IDS):c.849G>C (p.Val283=) rs147374356 0.00021
NM_000202.8(IDS):c.445T>G (p.Ser149Ala) rs146846763 0.00015
NM_000202.8(IDS):c.667G>A (p.Val223Ile) rs200784263 0.00012
NM_000202.8(IDS):c.957C>T (p.Asp319=) rs782488487 0.00011
NM_000202.8(IDS):c.881G>A (p.Arg294Gln) rs782445506 0.00010
NM_000202.8(IDS):c.1159G>A (p.Ala387Thr) rs376725292 0.00008
NM_000202.8(IDS):c.753C>T (p.Pro251=) rs782051908 0.00006
NM_000202.8(IDS):c.937C>T (p.Arg313Cys) rs201048643 0.00006
NM_000202.8(IDS):c.1158C>T (p.Ser386=) rs372340411 0.00005
NM_000202.8(IDS):c.851C>T (p.Pro284Leu) rs782286857 0.00005
NM_000202.8(IDS):c.868G>A (p.Val290Met) rs782479238 0.00005
NM_000202.8(IDS):c.894G>A (p.Gln298=) rs781812519 0.00005
NM_000202.8(IDS):c.450G>A (p.Pro150=) rs201892132 0.00004
NM_000202.8(IDS):c.684A>G (p.Pro228=) rs782561677 0.00003
NM_000202.8(IDS):c.1113G>A (p.Pro371=) rs146615651 0.00002
NM_000202.8(IDS):c.696C>T (p.Phe232=) rs782498858 0.00002
NM_000202.8(IDS):c.1143C>T (p.Leu381=) rs781805300 0.00001
NM_000202.8(IDS):c.1007-7G>C rs2124006476
NM_000202.8(IDS):c.419-16dup rs781852261
NM_000202.8(IDS):c.419-6del rs781852261
NM_000202.8(IDS):c.636G>A (p.Met212Ile)
NM_000202.8(IDS):c.781C>A (p.Pro261Thr) rs141720810
NM_000202.8(IDS):c.880-11del
NM_000202.8(IDS):c.880-11dup
NM_000202.8(IDS):c.880-4G>A
NM_000202.8(IDS):c.957C>A (p.Asp319Glu) rs782488487

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