ClinVar Miner

List of variants reported as benign for Mucopolysaccharidosis, MPS-II by Labcorp Genetics (formerly Invitae), Labcorp

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ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_000202.8(IDS):c.438C>T (p.Thr146=) rs1141608 0.31135
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.418+12T>C rs470986 0.00736
NM_000202.8(IDS):c.1269C>T (p.Pro423=) rs61736890 0.00513
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 0.00119
NM_000202.8(IDS):c.123C>G (p.Leu41=) rs146904022 0.00115
NM_000202.8(IDS):c.126C>T (p.Ile42=) rs146963087 0.00115
NM_000202.8(IDS):c.1181-13C>T rs188486717 0.00081
NM_000202.8(IDS):c.884A>G (p.Lys295Arg) rs113993953 0.00068
NM_000202.8(IDS):c.396G>A (p.Ser132=) rs147108245 0.00063
NM_000202.8(IDS):c.781C>G (p.Pro261Ala) rs141720810 0.00055
NM_000202.8(IDS):c.666C>T (p.Ala222=) rs201588028 0.00037
NM_000202.8(IDS):c.1074C>G (p.Pro358=) rs61736891 0.00034
NM_000202.8(IDS):c.104A>G (p.Asp35Gly) rs144081417 0.00020
NM_000202.8(IDS):c.849G>C (p.Val283=) rs147374356 0.00020
NM_000202.8(IDS):c.445T>G (p.Ser149Ala) rs146846763 0.00017
NM_000202.8(IDS):c.1490A>G (p.Tyr497Cys) rs142248439 0.00015
NM_000202.8(IDS):c.41G>A (p.Gly14Asp) rs373389352 0.00015
NM_000202.8(IDS):c.667G>A (p.Val223Ile) rs200784263 0.00015
NM_000202.8(IDS):c.727C>T (p.Pro243Ser) rs143474305 0.00015
NM_000202.8(IDS):c.103+7C>T rs369735286 0.00011
NM_000202.8(IDS):c.236C>G (p.Ala79Gly) rs368513342 0.00011
NM_000202.8(IDS):c.957C>T (p.Asp319=) rs782488487 0.00011
NM_000202.8(IDS):c.1499C>T (p.Thr500Ile) rs372205468 0.00010
NM_000202.8(IDS):c.881G>A (p.Arg294Gln) rs782445506 0.00010
NM_000202.8(IDS):c.1227G>A (p.Thr409=) rs201905166 0.00009
NM_000202.8(IDS):c.1159G>A (p.Ala387Thr) rs376725292 0.00008
NM_000202.8(IDS):c.162T>C (p.Tyr54=) rs141088021 0.00007
NM_000202.8(IDS):c.234T>C (p.Phe78=) rs782290556 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.23G>T (p.Arg8Leu) rs782621858 0.00005
NM_000202.8(IDS):c.450G>A (p.Pro150=) rs201892132 0.00005
NM_000202.8(IDS):c.753C>T (p.Pro251=) rs782051908 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.1290G>A (p.Glu430=) rs140633427 0.00004
NM_000202.8(IDS):c.301C>T (p.Arg101Cys) rs782738754 0.00004
NM_000202.8(IDS):c.696C>T (p.Phe232=) rs782498858 0.00004
NM_000202.8(IDS):c.27C>T (p.Gly9=) rs782412902 0.00003
NM_000202.8(IDS):c.684A>G (p.Pro228=) rs782561677 0.00003
NM_000202.8(IDS):c.894G>A (p.Gln298=) rs781812519 0.00003
NM_000202.8(IDS):c.1113G>A (p.Pro371=) rs146615651 0.00002
NM_000202.8(IDS):c.1181-14G>A rs200950988 0.00002
NM_000202.8(IDS):c.1181-15C>T rs199965368 0.00002
NM_000202.8(IDS):c.1347G>A (p.Glu449=) rs782690963 0.00002
NM_000202.8(IDS):c.177G>A (p.Val59=) rs782743276 0.00002
NM_000202.8(IDS):c.636G>A (p.Met212Ile) rs1557339525 0.00002
NM_000202.8(IDS):c.880-4G>A rs782623359 0.00002
NM_000202.8(IDS):c.1143C>T (p.Leu381=) rs781805300 0.00001
NM_000202.8(IDS):c.1327C>A (p.Arg443=) rs199422227 0.00001
NM_000202.8(IDS):c.13C>T (p.Arg5Trp) rs141900718 0.00001
NM_000202.8(IDS):c.418+14T>C rs781915630 0.00001
NM_000202.8(IDS):c.103+5C>T rs782108228
NM_000202.8(IDS):c.1548C>T (p.Asp516=) rs782433387
NM_000202.8(IDS):c.418+17A>G rs1210262255
NM_000202.8(IDS):c.419-16dup rs781852261
NM_000202.8(IDS):c.419-6del rs781852261
NM_000202.8(IDS):c.781C>A (p.Pro261Thr) rs141720810
NM_000202.8(IDS):c.880-11del rs781892166
NM_000202.8(IDS):c.880-11dup rs781892166
NM_000202.8(IDS):c.957C>A (p.Asp319Glu) rs782488487

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