ClinVar Miner

List of variants in gene FERMT1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 127
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HGVS dbSNP gnomAD frequency
NM_017671.5(FERMT1):c.1014C>T (p.Ser338=) rs138986656 0.00159
NM_017671.5(FERMT1):c.1627G>A (p.Val543Met) rs76933768 0.00061
NM_017671.5(FERMT1):c.637G>A (p.Glu213Lys) rs149092699 0.00055
NM_017671.5(FERMT1):c.756C>T (p.Asp252=) rs142628403 0.00044
NM_017671.5(FERMT1):c.306G>A (p.Pro102=) rs141850118 0.00037
NM_017671.5(FERMT1):c.882G>A (p.Glu294=) rs149893089 0.00027
NM_017671.5(FERMT1):c.293G>A (p.Arg98His) rs137862671 0.00026
NM_017671.5(FERMT1):c.1077G>A (p.Ala359=) rs34569233 0.00023
NM_017671.5(FERMT1):c.957+10C>A rs368444538 0.00022
NM_017671.5(FERMT1):c.2019C>T (p.Thr673=) rs368745513 0.00021
NM_017671.5(FERMT1):c.1594-6G>A rs6053893 0.00019
NM_017671.5(FERMT1):c.978G>A (p.Ser326=) rs201694674 0.00011
NM_017671.5(FERMT1):c.1167C>T (p.Phe389=) rs374069028 0.00006
NM_017671.5(FERMT1):c.1599C>T (p.Ala533=) rs774007627 0.00006
NM_017671.5(FERMT1):c.279G>A (p.Gln93=) rs150528781 0.00006
NM_017671.5(FERMT1):c.657C>T (p.Leu219=) rs150419419 0.00006
NM_017671.5(FERMT1):c.746+10C>T rs374779394 0.00004
NM_017671.5(FERMT1):c.958-18C>T rs781039429 0.00004
NM_017671.5(FERMT1):c.1617G>A (p.Ala539=) rs111823157 0.00003
NM_017671.5(FERMT1):c.1944C>T (p.Gly648=) rs570732725 0.00003
NM_017671.5(FERMT1):c.219C>T (p.Thr73=) rs574151559 0.00003
NM_017671.5(FERMT1):c.533-14C>T rs749711628 0.00003
NM_017671.5(FERMT1):c.958-17G>A rs752037149 0.00003
NM_017671.5(FERMT1):c.1038G>A (p.Ala346=) rs770494158 0.00002
NM_017671.5(FERMT1):c.1335C>T (p.Ala445=) rs751428620 0.00002
NM_017671.5(FERMT1):c.1372-11G>C rs762037034 0.00002
NM_017671.5(FERMT1):c.39G>A (p.Glu13=) rs748600328 0.00002
NM_017671.5(FERMT1):c.459C>T (p.Asp153=) rs769642349 0.00002
NM_017671.5(FERMT1):c.780A>G (p.Gln260=) rs754424986 0.00002
NM_017671.5(FERMT1):c.1140-16A>G rs749615948 0.00001
NM_017671.5(FERMT1):c.1265-10T>C rs1210125220 0.00001
NM_017671.5(FERMT1):c.1265-16G>C rs1279894861 0.00001
NM_017671.5(FERMT1):c.1278G>A (p.Val426=) rs146325251 0.00001
NM_017671.5(FERMT1):c.1372-8T>G rs774479044 0.00001
NM_017671.5(FERMT1):c.1620C>T (p.His540=) rs778002718 0.00001
NM_017671.5(FERMT1):c.1647C>T (p.Val549=) rs267606039 0.00001
NM_017671.5(FERMT1):c.1718+9A>G rs183621104 0.00001
NM_017671.5(FERMT1):c.1992C>T (p.Leu664=) rs184046854 0.00001
NM_017671.5(FERMT1):c.213G>A (p.Leu71=) rs1224521513 0.00001
NM_017671.5(FERMT1):c.240T>C (p.Tyr80=) rs550863008 0.00001
NM_017671.5(FERMT1):c.243G>A (p.Gly81=) rs764556729 0.00001
NM_017671.5(FERMT1):c.386-20T>A rs1294304701 0.00001
NM_017671.5(FERMT1):c.423G>A (p.Pro141=) rs41308076 0.00001
NM_017671.5(FERMT1):c.438T>C (p.Phe146=) rs762090385 0.00001
NM_017671.5(FERMT1):c.495A>C (p.Leu165=) rs1198608028 0.00001
NM_017671.5(FERMT1):c.746+11G>A rs370631532 0.00001
NM_017671.5(FERMT1):c.747-20C>G rs995062310 0.00001
NM_017671.5(FERMT1):c.834C>T (p.Phe278=) rs775613961 0.00001
NM_017671.5(FERMT1):c.84C>T (p.Asp28=) rs765106857 0.00001
NM_017671.5(FERMT1):c.105A>G (p.Gly35=)
NM_017671.5(FERMT1):c.1077G>T (p.Ala359=)
NM_017671.5(FERMT1):c.1089+118_1089+119del rs202086138
NM_017671.5(FERMT1):c.1089+8C>T rs755468837
NM_017671.5(FERMT1):c.1090-16_1090-13del
NM_017671.5(FERMT1):c.1104T>C (p.Asp368=)
NM_017671.5(FERMT1):c.1264+18C>T
NM_017671.5(FERMT1):c.1264+8T>A rs2123106863
NM_017671.5(FERMT1):c.1284T>C (p.Asp428=)
NM_017671.5(FERMT1):c.1302A>G (p.Arg434=)
NM_017671.5(FERMT1):c.1372-16C>T rs370927689
NM_017671.5(FERMT1):c.1372-6C>A
NM_017671.5(FERMT1):c.1404C>T (p.Cys468=)
NM_017671.5(FERMT1):c.1408T>C (p.Leu470=)
NM_017671.5(FERMT1):c.144A>G (p.Glu48=)
NM_017671.5(FERMT1):c.1467C>T (p.Ile489=) rs374391922
NM_017671.5(FERMT1):c.1473A>G (p.Ser491=)
NM_017671.5(FERMT1):c.1497C>T (p.Asn499=) rs760520937
NM_017671.5(FERMT1):c.151+12T>A rs770119324
NM_017671.5(FERMT1):c.151+14G>A
NM_017671.5(FERMT1):c.151+14G>C
NM_017671.5(FERMT1):c.152-19T>C
NM_017671.5(FERMT1):c.152-20T>C
NM_017671.5(FERMT1):c.152-5T>G
NM_017671.5(FERMT1):c.1593+15G>A
NM_017671.5(FERMT1):c.1593+7T>C
NM_017671.5(FERMT1):c.1594-11T>C
NM_017671.5(FERMT1):c.1594-14_1594-13del
NM_017671.5(FERMT1):c.15T>G (p.Thr5=)
NM_017671.5(FERMT1):c.1629G>A (p.Val543=)
NM_017671.5(FERMT1):c.1719-4T>C
NM_017671.5(FERMT1):c.1743C>T (p.Asp581=)
NM_017671.5(FERMT1):c.174C>T (p.Asp58=)
NM_017671.5(FERMT1):c.1800A>G (p.Pro600=)
NM_017671.5(FERMT1):c.1809A>T (p.Thr603=)
NM_017671.5(FERMT1):c.1818C>T (p.Phe606=) rs776343825
NM_017671.5(FERMT1):c.1857G>A (p.Arg619=)
NM_017671.5(FERMT1):c.1860+12G>A
NM_017671.5(FERMT1):c.1861-20T>C
NM_017671.5(FERMT1):c.1887C>G (p.Val629=)
NM_017671.5(FERMT1):c.1905C>T (p.Cys635=)
NM_017671.5(FERMT1):c.1908G>A (p.Leu636=)
NM_017671.5(FERMT1):c.1914A>G (p.Ala638=)
NM_017671.5(FERMT1):c.1944C>A (p.Gly648=)
NM_017671.5(FERMT1):c.1956C>T (p.Phe652=)
NM_017671.5(FERMT1):c.1968C>T (p.Arg656=)
NM_017671.5(FERMT1):c.2019C>G (p.Thr673=)
NM_017671.5(FERMT1):c.385+12G>A rs773446800
NM_017671.5(FERMT1):c.386-9T>C rs755234339
NM_017671.5(FERMT1):c.414G>A (p.Leu138=) rs539867893
NM_017671.5(FERMT1):c.465T>C (p.Asn155=)
NM_017671.5(FERMT1):c.532+10G>C rs780579097
NM_017671.5(FERMT1):c.533-13C>T
NM_017671.5(FERMT1):c.543T>C (p.Gly181=)
NM_017671.5(FERMT1):c.546A>G (p.Leu182=)
NM_017671.5(FERMT1):c.591A>T (p.Thr197=)
NM_017671.5(FERMT1):c.606C>T (p.Thr202=)
NM_017671.5(FERMT1):c.636G>A (p.Thr212=) rs773713545
NM_017671.5(FERMT1):c.636G>T (p.Thr212=)
NM_017671.5(FERMT1):c.72G>A (p.Glu24=) rs1983204513
NM_017671.5(FERMT1):c.738C>A (p.Leu246=)
NM_017671.5(FERMT1):c.746+12G>T
NM_017671.5(FERMT1):c.746+14T>A
NM_017671.5(FERMT1):c.746+15C>T
NM_017671.5(FERMT1):c.746+18T>C
NM_017671.5(FERMT1):c.747-17A>G
NM_017671.5(FERMT1):c.747-20C>T rs995062310
NM_017671.5(FERMT1):c.819A>G (p.Lys273=)
NM_017671.5(FERMT1):c.81A>G (p.Lys27=)
NM_017671.5(FERMT1):c.849+11T>A
NM_017671.5(FERMT1):c.849+17_849+21del
NM_017671.5(FERMT1):c.852T>C (p.Tyr284=) rs1982546087
NM_017671.5(FERMT1):c.918T>C (p.Asp306=)
NM_017671.5(FERMT1):c.927G>A (p.Glu309=)
NM_017671.5(FERMT1):c.93G>A (p.Leu31=)
NM_017671.5(FERMT1):c.957+10C>T
NM_017671.5(FERMT1):c.958-7A>G
NM_017671.5(FERMT1):c.981G>A (p.Leu327=)

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