ClinVar Miner

List of variants reported as uncertain significance for Inflammatory bowel disease

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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_000572.3(IL10):c.58C>T (p.Pro20Ser) rs141219090 0.00038
NM_000572.3(IL10):c.530G>A (p.Arg177Gln) rs376415487 0.00009
NM_000572.3(IL10):c.225+6A>G rs749041176 0.00008
NM_000572.3(IL10):c.343A>T (p.Asn115Tyr) rs150423829 0.00007
NM_000572.3(IL10):c.371G>A (p.Arg124Gln) rs201365412 0.00004
NM_000572.3(IL10):c.314T>G (p.Ile105Ser) rs372883095 0.00003
NM_000572.3(IL10):c.374G>A (p.Arg125His) rs374619208 0.00003
NM_000628.5(IL10RB):c.*365C>T rs886057005 0.00003
NM_000572.3(IL10):c.134G>A (p.Arg45Gln) rs550164520 0.00002
NM_000572.3(IL10):c.37C>A (p.Leu13Met) rs769236514 0.00002
NM_000572.3(IL10):c.121C>T (p.Leu41Phe) rs750010814 0.00001
NM_000572.3(IL10):c.274G>A (p.Glu92Lys) rs780612967 0.00001
NM_000572.3(IL10):c.301C>A (p.Gln101Lys) rs777582308 0.00001
NM_000572.3(IL10):c.320C>T (p.Ala107Val) rs755490123 0.00001
NM_000572.3(IL10):c.365G>A (p.Arg122Lys) rs371608920 0.00001
NM_000572.3(IL10):c.370C>T (p.Arg124Trp) rs746523858 0.00001
NM_000572.3(IL10):c.383G>T (p.Arg128Leu) rs760677075 0.00001
NM_000572.3(IL10):c.434C>T (p.Ala145Val) rs774072665 0.00001
NM_000572.3(IL10):c.444+6C>T rs749664677 0.00001
NM_000572.3(IL10):c.514A>G (p.Met172Val) rs768418064 0.00001
NM_000572.3(IL10):c.521T>C (p.Met174Thr) rs762496248 0.00001
NC_000001.10:g.(?_206941981)_(208391267_?)dup
NM_000572.3(IL10):c.100C>A (p.Pro34Thr) rs2102441015
NM_000572.3(IL10):c.112C>G (p.Pro38Ala)
NM_000572.3(IL10):c.118A>G (p.Met40Val)
NM_000572.3(IL10):c.137A>G (p.Asp46Gly)
NM_000572.3(IL10):c.209T>A (p.Leu70Ter) rs1558603013
NM_000572.3(IL10):c.241C>A (p.Gln81Lys) rs2102439318
NM_000572.3(IL10):c.257T>A (p.Met86Lys)
NM_000572.3(IL10):c.320C>A (p.Ala107Glu)
NM_000572.3(IL10):c.323A>G (p.His108Arg) rs1307541646
NM_000572.3(IL10):c.332C>T (p.Ser111Phe) rs1674812448
NM_000572.3(IL10):c.374G>T (p.Arg125Leu) rs374619208
NM_000572.3(IL10):c.378+6T>C
NM_000572.3(IL10):c.383G>A (p.Arg128Gln) rs760677075
NM_000572.3(IL10):c.386T>A (p.Phe129Tyr)
NM_000572.3(IL10):c.424G>C (p.Val142Leu)
NM_000572.3(IL10):c.443A>G (p.Lys148Arg)
NM_000572.3(IL10):c.46G>T (p.Val16Leu) rs1674878129
NM_000572.3(IL10):c.502A>G (p.Ile168Val) rs2102436707
NM_000572.3(IL10):c.503T>A (p.Ile168Lys)
NM_000572.3(IL10):c.507A>C (p.Glu169Asp) rs568879359
NM_000572.3(IL10):c.529C>T (p.Arg177Ter)
NM_000572.3(IL10):c.534C>A (p.Asn178Lys)
NM_000572.3(IL10):c.534C>G (p.Asn178Lys) rs771277922
NM_000572.3(IL10):c.62G>A (p.Gly21Asp)
NM_000572.3(IL10):c.71C>G (p.Thr24Ser) rs1674877288
NM_000572.3(IL10):c.92C>T (p.Thr31Ile)
NM_000572.3(IL10):c.94C>A (p.His32Asn) rs376787667
NM_000628.5(IL10RB):c.*593TC[1] rs886057007
NM_000628.5(IL10RB):c.*616del rs5843596
NM_001631.5(ALPI):c.406C>T (p.Arg136Cys)
NM_001631.5(ALPI):c.83C>T (p.Pro28Leu)

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