ClinVar Miner

List of variants in gene F11 reported by UniProtKB/Swiss-Prot

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.809A>T (p.Lys270Ile) rs121965070 0.00055
NM_000128.4(F11):c.683G>A (p.Arg228Gln) rs281875246 0.00006
NM_000128.4(F11):c.943G>A (p.Glu315Lys) rs281875257 0.00006
NM_000128.4(F11):c.127G>A (p.Ala43Thr) rs281875264 0.00004
NM_000128.4(F11):c.723C>G (p.Phe241Leu) rs281875265 0.00004
NM_000128.4(F11):c.1724C>T (p.Ser575Leu) rs281875250 0.00003
NM_000128.4(F11):c.1853T>G (p.Ile618Ser) rs281875276 0.00002
NM_000128.4(F11):c.100G>C (p.Asp34His) rs281875267 0.00001
NM_000128.4(F11):c.1021G>A (p.Glu341Lys) rs281875270 0.00001
NM_000128.4(F11):c.1207G>A (p.Val403Met) rs281875266 0.00001
NM_000128.4(F11):c.137G>T (p.Cys46Phe) rs281875271 0.00001
NM_000128.4(F11):c.1517A>G (p.Asp506Gly) rs281875258 0.00001
NM_000128.4(F11):c.1578C>G (p.Asp526Glu) rs281875263 0.00001
NM_000128.4(F11):c.1693G>A (p.Glu565Lys) rs281875275 0.00001
NM_000128.4(F11):c.1789G>A (p.Glu597Lys) rs281875251 0.00001
NM_000128.4(F11):c.188C>T (p.Ala63Val) rs281875244 0.00001
NM_000128.4(F11):c.302A>G (p.Lys101Arg) rs281875272 0.00001
NM_000128.4(F11):c.419G>A (p.Cys140Tyr) rs281875256 0.00001
NM_000128.4(F11):c.959T>C (p.Leu320Pro) rs281875268 0.00001
NM_000128.4(F11):c.965C>T (p.Thr322Ile) rs281875269 0.00001
NM_000128.4(F11):c.1079T>C (p.Leu360Pro) rs281875254
NM_000128.4(F11):c.1201T>C (p.Trp401Arg) rs281875262
NM_000128.4(F11):c.1361T>A (p.Ile454Lys) rs281875241
NM_000128.4(F11):c.1442T>G (p.Ile481Ser) rs281875242
NM_000128.4(F11):c.1507T>C (p.Ser503Pro) rs140068026
NM_000128.4(F11):c.151A>C (p.Thr51Pro) rs281875243
NM_000128.4(F11):c.152C>T (p.Thr51Ile) rs281875252
NM_000128.4(F11):c.1531T>C (p.Tyr511His) rs281875278
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.1822T>C (p.Tyr608His) rs281875255
NM_000128.4(F11):c.452A>G (p.Tyr151Cys) rs281875273
NM_000128.4(F11):c.664G>T (p.Asp222Tyr) rs281875245
NM_000128.4(F11):c.738G>C (p.Trp246Cys) rs281875279
NM_000128.4(F11):c.755G>C (p.Arg252Thr) rs281875260
NM_000128.4(F11):c.764G>A (p.Cys255Tyr) rs281875277
NM_000128.4(F11):c.788G>A (p.Gly263Glu) rs281875274
NM_000128.4(F11):c.827C>G (p.Ser276Cys) rs281875247
NM_000128.4(F11):c.830G>A (p.Gly277Asp) rs281875248
NM_000128.4(F11):c.94G>A (p.Gly32Arg) rs281875259
NM_000128.4(F11):c.992C>T (p.Thr331Ile) rs281875253

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