ClinVar Miner

List of variants reported as pathogenic for Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_003620.4(PPM1D):c.1654C>T (p.Arg552Ter) rs779070661 0.00004
NM_003620.4(PPM1D):c.1714C>T (p.Arg572Ter) rs765769406 0.00002
NM_003620.4(PPM1D):c.1281G>A (p.Trp427Ter) rs1064797099 0.00001
NM_003620.4(PPM1D):c.1216del (p.Thr406fs) rs747947002
NM_003620.4(PPM1D):c.1221T>A (p.Cys407Ter) rs189669693
NM_003620.4(PPM1D):c.1248_1252del (p.Pro417fs) rs1567977657
NM_003620.4(PPM1D):c.1250dup (p.Pro418fs) rs1064797100
NM_003620.4(PPM1D):c.1259dup (p.Ser421fs) rs1598413570
NM_003620.4(PPM1D):c.1270dup (p.Glu424fs) rs1064797098
NM_003620.4(PPM1D):c.1278dup (p.Trp427fs) rs2031551825
NM_003620.4(PPM1D):c.1280G>A (p.Trp427Ter)
NM_003620.4(PPM1D):c.1288del (p.Arg429_Val430insTer)
NM_003620.4(PPM1D):c.1388_1389delinsA (p.Gly463fs) rs2031555258
NM_003620.4(PPM1D):c.1535del (p.Asn512fs) rs763475304

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