ClinVar Miner

List of variants in gene F11 studied for not specified

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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.1191T>C (p.Gly397=) rs5970 0.16228
NM_000128.4(F11):c.801A>G (p.Thr267=) rs5974 0.16101
NM_000128.4(F11):c.1812G>T (p.Arg604=) rs5971 0.06917
NM_000128.4(F11):c.429C>T (p.Asp143=) rs5973 0.06445
NM_000128.4(F11):c.1839G>A (p.Glu613=) rs5976 0.04596
NM_000128.4(F11):c.1304+12G>A rs116667976 0.00295
NM_000128.4(F11):c.1305-9G>T rs4253426 0.00153
NM_000128.4(F11):c.127G>A (p.Ala43Thr) rs281875264 0.00004
NM_000128.4(F11):c.452A>G (p.Tyr151Cys) rs281875273 0.00002
NM_000128.4(F11):c.683G>A (p.Arg228Gln) rs281875246 0.00002
NM_000128.4(F11):c.1103G>C (p.Gly368Ala) rs748926718 0.00001
NM_000128.4(F11):c.1289C>T (p.Ala430Val) rs121965068 0.00001
NM_000128.4(F11):c.1609A>T (p.Ile537Leu) rs199911285 0.00001
NM_000128.4(F11):c.1693G>A (p.Glu565Lys) rs281875275 0.00001
NM_000128.4(F11):c.365G>A (p.Gly122Asp) rs369650561 0.00001
NM_000128.4(F11):c.374A>G (p.Tyr125Cys) rs1554082187 0.00001
NM_000128.4(F11):c.1106A>C (p.Tyr369Ser) rs1580090672
NM_000128.4(F11):c.1211C>A (p.Thr404Asn) rs121965067
NM_000128.4(F11):c.126C>A (p.Ser42Arg)
NM_000128.4(F11):c.1288G>T (p.Ala430Ser) rs753909969
NM_000128.4(F11):c.1305-10T>A rs1233980263
NM_000128.4(F11):c.1326G>C (p.Leu442Phe)
NM_000128.4(F11):c.152C>T (p.Thr51Ile) rs281875252
NM_000128.4(F11):c.1541G>T (p.Cys514Phe) rs281875249
NM_000128.4(F11):c.159C>A (p.His53Gln) rs281875261
NM_000128.4(F11):c.1716+12T>C rs371232210
NM_000128.4(F11):c.296C>A (p.Ser99Tyr)
NM_000128.4(F11):c.94G>A (p.Gly32Arg) rs281875259

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