ClinVar Miner

List of variants in gene MYT1L reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_001303052.2(MYT1L):c.1716C>T (p.Ser572=) rs61743488 0.00354
NM_001303052.2(MYT1L):c.153-7T>A rs191453776 0.00208
NM_001303052.2(MYT1L):c.2922C>T (p.Ser974=) rs200125635 0.00129
NM_001303052.2(MYT1L):c.1512C>T (p.Ser504=) rs148988262 0.00107
NM_001303052.2(MYT1L):c.657C>T (p.Ala219=) rs370129180 0.00047
NM_001303052.2(MYT1L):c.915C>T (p.Pro305=) rs183694893 0.00045
NM_001303052.2(MYT1L):c.1410G>A (p.Pro470=) rs373769933 0.00040
NM_001303052.2(MYT1L):c.1422C>T (p.Pro474=) rs199944271 0.00034
NM_001303052.2(MYT1L):c.3039C>T (p.Asp1013=) rs371203153 0.00029
NM_001303052.2(MYT1L):c.2520T>C (p.Thr840=) rs201805139 0.00022
NM_001303052.2(MYT1L):c.372C>T (p.Asp124=) rs532643748 0.00012
NM_001303052.2(MYT1L):c.48G>A (p.Gly16=) rs377141211 0.00010
NM_001303052.2(MYT1L):c.1764G>A (p.Lys588=) rs373834403 0.00009
NM_001303052.2(MYT1L):c.1200G>A (p.Ala400=) rs373977335 0.00007
NM_001303052.2(MYT1L):c.387G>A (p.Arg129=) rs138932120 0.00006
NM_001303052.2(MYT1L):c.111C>T (p.Asp37=) rs546427673 0.00005
NM_001303052.2(MYT1L):c.3080+8343G>A rs1346976183 0.00005
NM_001303052.2(MYT1L):c.995A>G (p.Asn332Ser) rs199856266 0.00005
NM_001303052.2(MYT1L):c.2910G>A (p.Ala970=) rs745509665 0.00004
NM_001303052.2(MYT1L):c.1890G>A (p.Pro630=) rs745509992 0.00002
NM_001303052.2(MYT1L):c.3096G>A (p.Pro1032=) rs565637135 0.00002
NM_001303052.2(MYT1L):c.1548C>T (p.His516=) rs750963882 0.00001
NM_001303052.2(MYT1L):c.2346G>A (p.Pro782=) rs557858474 0.00001
NM_001303052.2(MYT1L):c.1053G>T (p.Pro351=) rs13399855
NM_001303052.2(MYT1L):c.1073G>A (p.Arg358His)
NM_001303052.2(MYT1L):c.1296C>G (p.Thr432=)
NM_001303052.2(MYT1L):c.1803G>A (p.Ser601=)
NM_001303052.2(MYT1L):c.1875C>T (p.Val625=)
NM_001303052.2(MYT1L):c.216T>C (p.Ala72=)
NM_001303052.2(MYT1L):c.2486G>A (p.Arg829Gln)
NM_001303052.2(MYT1L):c.2801A>G (p.Lys934Arg)
NM_001303052.2(MYT1L):c.2931G>A (p.Gly977=)
NM_001303052.2(MYT1L):c.3075C>T (p.His1025=)
NM_001303052.2(MYT1L):c.3080+1360A>G
NM_001303052.2(MYT1L):c.3080+1369A>G
NM_001303052.2(MYT1L):c.3080+4019C>T
NM_001303052.2(MYT1L):c.3080+4168_3080+4200del
NM_001303052.2(MYT1L):c.3080+4355_3080+4387del rs1558695136
NM_001303052.2(MYT1L):c.3080+8229G>A
NM_001303052.2(MYT1L):c.3080+8283T>C
NM_001303052.2(MYT1L):c.3080+8315G>A
NM_001303052.2(MYT1L):c.3285G>A (p.Thr1095=)
NM_001303052.2(MYT1L):c.687C>G (p.Thr229=)

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