ClinVar Miner

List of variants in gene F11 reported as not provided

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Total variants: 42
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HGVS dbSNP
NM_000128.3(F11):c.100G>C (p.Asp34His) rs281875267
NM_000128.3(F11):c.1021G>A (p.Glu341Lys) rs281875270
NM_000128.3(F11):c.1079T>C (p.Leu360Pro) rs281875254
NM_000128.3(F11):c.1201T>C (p.Trp401Arg) rs281875262
NM_000128.3(F11):c.1207G>A (p.Val403Met) rs281875266
NM_000128.3(F11):c.127G>A (p.Ala43Thr) rs281875264
NM_000128.3(F11):c.1361T>A (p.Ile454Lys) rs281875241
NM_000128.3(F11):c.137G>T (p.Cys46Phe) rs281875271
NM_000128.3(F11):c.1442T>G (p.Ile481Ser) rs281875242
NM_000128.3(F11):c.1507T>C (p.Ser503Pro) rs140068026
NM_000128.3(F11):c.1517A>G (p.Asp506Gly) rs281875258
NM_000128.3(F11):c.151A>C (p.Thr51Pro) rs281875243
NM_000128.3(F11):c.152C>T (p.Thr51Ile) rs281875252
NM_000128.3(F11):c.1531T>C (p.Tyr511His) rs281875278
NM_000128.3(F11):c.1541G>T (p.Cys514Phe) rs281875249
NM_000128.3(F11):c.1578C>G (p.Asp526Glu) rs281875263
NM_000128.3(F11):c.159C>A (p.His53Gln) rs281875261
NM_000128.3(F11):c.1693G>A (p.Glu565Lys) rs281875275
NM_000128.3(F11):c.1724C>T (p.Ser575Leu) rs281875250
NM_000128.3(F11):c.1789G>A (p.Glu597Lys) rs281875251
NM_000128.3(F11):c.1822T>C (p.Tyr608His) rs281875255
NM_000128.3(F11):c.1853T>G (p.Ile618Ser) rs281875276
NM_000128.3(F11):c.188C>T (p.Ala63Val) rs281875244
NM_000128.3(F11):c.302A>G (p.Lys101Arg) rs281875272
NM_000128.3(F11):c.419G>A (p.Cys140Tyr) rs281875256
NM_000128.3(F11):c.452A>G (p.Tyr151Cys) rs281875273
NM_000128.3(F11):c.664G>T (p.Asp222Tyr) rs281875245
NM_000128.3(F11):c.683G>A (p.Arg228Gln) rs281875246
NM_000128.3(F11):c.723C>G (p.Phe241Leu) rs281875265
NM_000128.3(F11):c.738G>C (p.Trp246Cys) rs281875279
NM_000128.3(F11):c.755G>C (p.Arg252Thr) rs281875260
NM_000128.3(F11):c.764G>A (p.Cys255Tyr) rs281875277
NM_000128.3(F11):c.788G>A (p.Gly263Glu) rs281875274
NM_000128.3(F11):c.809A>T (p.Lys270Ile) rs121965070
NM_000128.3(F11):c.827C>G (p.Ser276Cys) rs281875247
NM_000128.3(F11):c.830G>A (p.Gly277Asp) rs281875248
NM_000128.3(F11):c.943G>A (p.Glu315Lys) rs281875257
NM_000128.3(F11):c.94G>A (p.Gly32Arg) rs281875259
NM_000128.3(F11):c.959T>C (p.Leu320Pro) rs281875268
NM_000128.3(F11):c.965C>T (p.Thr322Ile) rs281875269
NM_000128.3(F11):c.992C>T (p.Thr331Ile) rs281875253
NM_000128.4(F11):c.1178C>T (p.Ala393Val)

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