ClinVar Miner

List of variants in gene F11 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 32
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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 0.16187
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.1016G>T (p.Cys339Phe) rs5967 0.00586
NM_000128.4(F11):c.*1A>G rs143899287 0.00378
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.663C>T (p.Pro221=) rs142846329 0.00120
NM_000128.4(F11):c.403G>T (p.Glu135Ter) rs121965063 0.00066
NM_000128.4(F11):c.901T>C (p.Phe301Leu) rs121965064 0.00065
NM_000128.4(F11):c.866-9G>A rs200218867 0.00025
NM_000128.4(F11):c.126C>T (p.Ser42=) rs754973084 0.00024
NM_000128.4(F11):c.1179G>A (p.Ala393=) rs145927314 0.00016
NM_000128.4(F11):c.1200G>A (p.Pro400=) rs150377265 0.00007
NM_000128.4(F11):c.325+1G>A rs140190776 0.00004
NM_000128.4(F11):c.687C>T (p.Ile229=) rs150644991 0.00004
NM_000128.4(F11):c.1135+5G>A rs758515608 0.00003
NM_000128.4(F11):c.1489C>T (p.Arg497Ter) rs375422404 0.00003
NM_000128.4(F11):c.1853T>G (p.Ile618Ser) rs281875276 0.00002
NM_000128.4(F11):c.755+2T>C rs1220869989 0.00001
NC_000004.12:g.186265849A>G
NM_000128.4(F11):c.1075del (p.Ile359fs) rs786204429
NM_000128.4(F11):c.1136-1G>A
NM_000128.4(F11):c.1207G>T (p.Val403Leu)
NM_000128.4(F11):c.1313C>A (p.Ser438Ter) rs786204724
NM_000128.4(F11):c.1577-1G>C
NM_000128.4(F11):c.1716+12T>C rs371232210
NM_000128.4(F11):c.26A>G (p.His9Arg)
NM_000128.4(F11):c.456C>A (p.Ala152=)
NM_000128.4(F11):c.595+11A>G

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