ClinVar Miner

List of variants in gene DEPDC5 reported as likely pathogenic for not provided

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Gene type:
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Total variants: 15
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GRCh37/hg19 22q12.2(chr22:32150908-32156688)x1
GRCh37/hg19 22q12.2(chr22:32164800-32164849)x1
NM_001242896.3(DEPDC5):c.1550_1565dup (p.Asp522delinsGluGluProGlyPheTer)
NM_001242896.3(DEPDC5):c.2413del (p.Gln805fs)
NM_001242896.3(DEPDC5):c.944_945del (p.Asn315fs) rs1601935630
NM_001242896.3(DEPDC5):c.999_1000del (p.Val334fs) rs1601969933
NM_001242897.2(DEPDC5):c.1474C>T (p.Arg492Ter) rs1057519107
NM_001242897.2(DEPDC5):c.1870+2315C>T rs780960812
NM_001242897.2(DEPDC5):c.1870+2364dup rs1475605360
NM_001242897.2(DEPDC5):c.3262_3263dup (p.Thr1089fs) rs1555914806
NM_001242897.2(DEPDC5):c.388C>T (p.Gln130Ter) rs1569512941
NM_001242897.2(DEPDC5):c.4219+1G>A rs1555942720
NM_001242897.2(DEPDC5):c.562+1G>A rs1057524233
NM_001242897.2(DEPDC5):c.58+5G>C rs1064794917
NM_001242897.2(DEPDC5):c.946+1G>A rs1556608580

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