ClinVar Miner

List of variants in gene IL10 studied for Inflammatory bowel disease

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_000572.3(IL10):c.378+284G>T rs3024493 0.10942
NM_000572.3(IL10):c.530G>A (p.Arg177Gln) rs376415487 0.00009
NM_000572.3(IL10):c.379-19T>G rs759391400 0.00004
NM_000572.3(IL10):c.383G>T (p.Arg128Leu) rs760677075 0.00001
NM_000572.3(IL10):c.393C>T (p.Pro131=) rs1229974502 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
NM_000572.3(IL10):c.379-10del rs2102437972
NM_000572.3(IL10):c.379-16C>T
NM_000572.3(IL10):c.379-17T>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.414C>G (p.Ala138=)
NM_000572.3(IL10):c.424G>C (p.Val142Leu)
NM_000572.3(IL10):c.443A>G (p.Lys148Arg)
NM_000572.3(IL10):c.444+17G>A
NM_000572.3(IL10):c.444+20G>A
NM_000572.3(IL10):c.444+8T>C
NM_000572.3(IL10):c.445-8C>T
NM_000572.3(IL10):c.471C>A (p.Ala157=) rs1674735790
NM_000572.3(IL10):c.471C>T (p.Ala157=)
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.510C>T (p.Ala170=) rs142093260
NM_000572.3(IL10):c.513C>T (p.Tyr171=) rs1572537757
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

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