List of variants in gene DEPDC5 reported as uncertain significance by New York Genome Center

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.161A>C (p.Gln54Pro)	rs201312113	0.00019
NM_001242896.3(DEPDC5):c.2576C>T (p.Thr859Met)	rs200744555	0.00007
NM_001242896.3(DEPDC5):c.338A>T (p.Asp113Val)	rs529069517	0.00004
NM_001242896.3(DEPDC5):c.572A>G (p.Tyr191Cys)	rs749809456	0.00002
NM_001242896.3(DEPDC5):c.1081+4A>G	rs757563918
NM_001242896.3(DEPDC5):c.1274T>C (p.Leu425Pro)	rs2148665735
NM_001242896.3(DEPDC5):c.1640G>C (p.Ser547Thr)	rs1483477312
NM_001242896.3(DEPDC5):c.1655C>G (p.Thr552Ser)	rs2088928378
NM_001242896.3(DEPDC5):c.4627C>T (p.Arg1543Trp)	rs780294726

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