ClinVar Miner

List of variants in gene MYT1L reported as uncertain significance for not provided

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Gene type:
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Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_001303052.2(MYT1L):c.568A>G (p.Asn190Asp) rs1164310970 0.00004
NM_001303052.2(MYT1L):c.1325C>T (p.Thr442Met) rs754747899 0.00002
NM_001303052.2(MYT1L):c.3081-15_3081-8dup rs779563732 0.00002
NM_001303052.2(MYT1L):c.1947C>T (p.Asn649=) rs765607514 0.00001
NM_001303052.2(MYT1L):c.2348G>A (p.Arg783Gln) rs2048553228 0.00001
NM_001303052.2(MYT1L):c.2689G>A (p.Ala897Thr) rs370121424 0.00001
NM_001303052.2(MYT1L):c.2881G>A (p.Gly961Ser) rs1443529083 0.00001
NM_001303052.2(MYT1L):c.317A>G (p.Glu106Gly) rs1411503507 0.00001
NM_001303052.2(MYT1L):c.634G>A (p.Ala212Thr) rs1277588922 0.00001
NM_001303052.2(MYT1L):c.672A>C (p.Glu224Asp) rs961550417 0.00001
NM_001303052.2(MYT1L):c.835A>G (p.Asn279Asp) rs1279364314 0.00001
NM_001303052.2(MYT1L):c.925G>A (p.Gly309Arg) rs781602277 0.00001
GRCh37/hg19 2p25.3(chr2:1798393-2162086)x3
GRCh37/hg19 2p25.3(chr2:1920627-2044260)x3
GRCh37/hg19 2p25.3(chr2:2138672-2204279)x1
GRCh37/hg19 2p25.3(chr2:2310845-2355682)x1
NM_001303052.2(MYT1L):c.1-9_1-6del
NM_001303052.2(MYT1L):c.1037C>T (p.Pro346Leu)
NM_001303052.2(MYT1L):c.1072C>T (p.Arg358Cys) rs192615880
NM_001303052.2(MYT1L):c.107G>A (p.Cys36Tyr)
NM_001303052.2(MYT1L):c.113G>A (p.Gly38Asp) rs2149488963
NM_001303052.2(MYT1L):c.1183G>A (p.Val395Met)
NM_001303052.2(MYT1L):c.1211G>C (p.Gly404Ala) rs370168626
NM_001303052.2(MYT1L):c.122A>G (p.His41Arg)
NM_001303052.2(MYT1L):c.1252G>A (p.Asp418Asn) rs1331223402
NM_001303052.2(MYT1L):c.134A>G (p.Lys45Arg)
NM_001303052.2(MYT1L):c.1457A>G (p.His486Arg)
NM_001303052.2(MYT1L):c.1468C>T (p.Pro490Ser)
NM_001303052.2(MYT1L):c.1483G>A (p.Asp495Asn)
NM_001303052.2(MYT1L):c.149G>A (p.Arg50Lys) rs2149488795
NM_001303052.2(MYT1L):c.157T>C (p.Tyr53His)
NM_001303052.2(MYT1L):c.1631A>G (p.His544Arg) rs1219808741
NM_001303052.2(MYT1L):c.173C>T (p.Ala58Val)
NM_001303052.2(MYT1L):c.1862A>G (p.Tyr621Cys) rs765731360
NM_001303052.2(MYT1L):c.1877C>T (p.Pro626Leu)
NM_001303052.2(MYT1L):c.1915G>A (p.Glu639Lys)
NM_001303052.2(MYT1L):c.2008A>G (p.Ile670Val)
NM_001303052.2(MYT1L):c.2012C>A (p.Ser671Tyr) rs2148959044
NM_001303052.2(MYT1L):c.2052C>G (p.Asp684Glu)
NM_001303052.2(MYT1L):c.2063G>C (p.Ser688Thr)
NM_001303052.2(MYT1L):c.2063GCA[3] (p.Ser691del)
NM_001303052.2(MYT1L):c.2074_2082del (p.Thr692_Ser694del) rs2048979784
NM_001303052.2(MYT1L):c.2075_2104del (p.Thr692_Ser701del) rs2148877512
NM_001303052.2(MYT1L):c.2084A>G (p.Tyr695Cys)
NM_001303052.2(MYT1L):c.2107C>G (p.Leu703Val)
NM_001303052.2(MYT1L):c.2123G>C (p.Gly708Ala)
NM_001303052.2(MYT1L):c.2127C>G (p.Ser709Arg) rs2148877167
NM_001303052.2(MYT1L):c.2141_2149del (p.Thr714_Ser716del) rs1553300314
NM_001303052.2(MYT1L):c.2201C>T (p.Thr734Ile)
NM_001303052.2(MYT1L):c.224G>A (p.Arg75Gln)
NM_001303052.2(MYT1L):c.2257A>C (p.Lys753Gln)
NM_001303052.2(MYT1L):c.2318T>C (p.Leu773Pro)
NM_001303052.2(MYT1L):c.2333A>G (p.Asn778Ser)
NM_001303052.2(MYT1L):c.2345C>A (p.Pro782Gln) rs749429732
NM_001303052.2(MYT1L):c.2393C>G (p.Pro798Arg)
NM_001303052.2(MYT1L):c.2396A>C (p.Gln799Pro) rs2148853100
NM_001303052.2(MYT1L):c.2422T>C (p.Cys808Arg)
NM_001303052.2(MYT1L):c.2452G>A (p.Asp818Asn) rs2048539766
NM_001303052.2(MYT1L):c.2458C>T (p.Pro820Ser) rs1064793641
NM_001303052.2(MYT1L):c.2474A>G (p.Lys825Arg)
NM_001303052.2(MYT1L):c.2489G>A (p.Arg830Lys) rs2148851905
NM_001303052.2(MYT1L):c.2560A>G (p.Arg854Gly) rs2148838167
NM_001303052.2(MYT1L):c.2573G>A (p.Gly858Glu)
NM_001303052.2(MYT1L):c.2642C>G (p.Thr881Ser)
NM_001303052.2(MYT1L):c.2663C>T (p.Ala888Val)
NM_001303052.2(MYT1L):c.26G>A (p.Arg9Gln)
NM_001303052.2(MYT1L):c.2752G>A (p.Gly918Ser)
NM_001303052.2(MYT1L):c.2770C>T (p.Arg924Trp)
NM_001303052.2(MYT1L):c.2872G>A (p.Gly958Arg)
NM_001303052.2(MYT1L):c.289G>A (p.Glu97Lys)
NM_001303052.2(MYT1L):c.2972A>G (p.Asn991Ser)
NM_001303052.2(MYT1L):c.304_306del (p.Lys102del)
NM_001303052.2(MYT1L):c.3077G>A (p.Arg1026His)
NM_001303052.2(MYT1L):c.3080+1356A>G
NM_001303052.2(MYT1L):c.3080+1473G>A
NM_001303052.2(MYT1L):c.3080+1538G>A
NM_001303052.2(MYT1L):c.3080+8229G>T
NM_001303052.2(MYT1L):c.310G>A (p.Glu104Lys) rs2149264115
NM_001303052.2(MYT1L):c.3175A>G (p.Ile1059Val)
NM_001303052.2(MYT1L):c.3200A>T (p.Gln1067Leu)
NM_001303052.2(MYT1L):c.3214A>C (p.Ile1072Leu)
NM_001303052.2(MYT1L):c.3236A>G (p.Asn1079Ser)
NM_001303052.2(MYT1L):c.32G>T (p.Arg11Leu)
NM_001303052.2(MYT1L):c.3358G>C (p.Glu1120Gln) rs2147786857
NM_001303052.2(MYT1L):c.3374G>A (p.Ser1125Asn)
NM_001303052.2(MYT1L):c.3393C>A (p.Ser1131Arg) rs1298337593
NM_001303052.2(MYT1L):c.3476A>G (p.Tyr1159Cys) rs2032160927
NM_001303052.2(MYT1L):c.348G>T (p.Glu116Asp)
NM_001303052.2(MYT1L):c.3530_3531del (p.Ile1177fs) rs2147782557
NM_001303052.2(MYT1L):c.3537G>C (p.Gln1179His)
NM_001303052.2(MYT1L):c.3547G>A (p.Gly1183Arg)
NM_001303052.2(MYT1L):c.376G>A (p.Glu126Lys)
NM_001303052.2(MYT1L):c.403_414del (p.Ile135_Glu138del)
NM_001303052.2(MYT1L):c.43A>G (p.Lys15Glu)
NM_001303052.2(MYT1L):c.456_461del (p.Glu166_Glu167del)
NM_001303052.2(MYT1L):c.459AGAGGA[3] (p.Glu167_Asn168insGluGlu)
NM_001303052.2(MYT1L):c.465_473del (p.Glu165_Glu167del) rs779800803
NM_001303052.2(MYT1L):c.560A>T (p.Asp187Val)
NM_001303052.2(MYT1L):c.68C>G (p.Pro23Arg)
NM_001303052.2(MYT1L):c.706G>C (p.Asp236His) rs1003039613
NM_001303052.2(MYT1L):c.744G>C (p.Glu248Asp)
NM_001303052.2(MYT1L):c.805G>A (p.Ala269Thr)
NM_001303052.2(MYT1L):c.845A>G (p.Asp282Gly)
NM_001303052.2(MYT1L):c.860A>G (p.Asp287Gly) rs2149108719
NM_001303052.2(MYT1L):c.870GCA[1] (p.Gln292del)

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