List of variants in gene DEPDC5 reported as pathogenic by Bioinformatics Core, Luxembourg Center for Systems Biomedicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.2135C>T (p.Ser712Phe)	rs16989535	0.02396
NM_001242896.3(DEPDC5):c.2020C>T (p.Arg674Cys)	rs181347577	0.00218
NM_001242896.3(DEPDC5):c.3265-3C>T	rs371377906	0.00108
NM_001242896.3(DEPDC5):c.3241A>C (p.Thr1081Pro)	rs142540948	0.00017
NM_001242896.3(DEPDC5):c.2066A>C (p.Glu689Ala)	rs370940232	0.00011
NM_001242896.3(DEPDC5):c.-57G>C	rs1383795440	0.00001
NM_001242896.3(DEPDC5):c.268G>A (p.Val90Ile)	rs768456731	0.00001
NM_001242896.3(DEPDC5):c.2492_2493insAGA (p.Ser831delinsArgAsp)	rs1555897392
NM_001242896.3(DEPDC5):c.3444del (p.Ile1148fs)	rs886039266
NM_001242896.3(DEPDC5):c.3484A>G (p.Ser1162Gly)	rs886039280
NM_001242896.3(DEPDC5):c.814G>T (p.Val272Leu)	rs187334123

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