List of variants in gene DEPDC5 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 40

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.2020C>T (p.Arg674Cys)	rs181347577	0.00218
NM_001242896.3(DEPDC5):c.3683T>C (p.Ile1228Thr)	rs200653339	0.00200
NM_001242896.3(DEPDC5):c.1321A>G (p.Thr441Ala)	rs199749859	0.00162
NM_001242896.3(DEPDC5):c.1330G>A (p.Gly444Arg)	rs201394709	0.00071
NM_001242896.3(DEPDC5):c.2354+28C>T	rs192889355	0.00071
NM_001242896.3(DEPDC5):c.3567A>G (p.Thr1189=)	rs142197878	0.00063
NM_001242896.3(DEPDC5):c.1525C>T (p.Arg509Cys)	rs202083639	0.00049
NM_001242896.3(DEPDC5):c.2354+48G>A	rs199622220	0.00045
NM_001242896.3(DEPDC5):c.3315C>T (p.Ser1105=)	rs371969641	0.00037
NM_001242896.3(DEPDC5):c.1290C>T (p.Pro430=)	rs201202102	0.00027
NM_001242896.3(DEPDC5):c.363+6_363+7del	rs748242785	0.00027
NM_001242896.3(DEPDC5):c.3021G>T (p.Arg1007=)	rs201690337	0.00024
NM_001242896.3(DEPDC5):c.1353C>T (p.Asn451=)	rs377336412	0.00018
NM_001242896.3(DEPDC5):c.3241A>C (p.Thr1081Pro)	rs142540948	0.00017
NM_001242896.3(DEPDC5):c.2784C>T (p.Ala928=)	rs201146392	0.00011
NM_001242896.3(DEPDC5):c.2973G>A (p.Glu991=)	rs370906184	0.00008
NM_001242896.3(DEPDC5):c.609A>G (p.Leu203=)	rs200639727	0.00007
NM_001242896.3(DEPDC5):c.842A>T (p.Tyr281Phe)	rs200797928	0.00006
NM_001242896.3(DEPDC5):c.1082-3T>A	rs780547994	0.00005
NM_001242896.3(DEPDC5):c.1509C>T (p.Ser503=)	rs376217381	0.00005
NM_001242896.3(DEPDC5):c.2592G>A (p.Thr864=)	rs763764167	0.00004
NM_001242896.3(DEPDC5):c.3624G>A (p.Ala1208=)	rs367828073	0.00004
NM_001242896.3(DEPDC5):c.3030C>T (p.Thr1010=)	rs548885626	0.00003
NM_001242896.3(DEPDC5):c.3225C>T (p.Ser1075=)	rs757534228	0.00003
NM_001242896.3(DEPDC5):c.3366C>T (p.Asp1122=)	rs375702574	0.00003
NM_001242896.3(DEPDC5):c.4437G>A (p.Arg1479=)	rs1057522689	0.00003
NM_001242896.3(DEPDC5):c.2286C>T (p.Asp762=)	rs200465447	0.00002
NM_001242896.3(DEPDC5):c.504G>A (p.Ser168=)	rs577652236	0.00002
NM_001242896.3(DEPDC5):c.2019C>G (p.Ser673=)	rs372975881	0.00001
NM_001242896.3(DEPDC5):c.2633+7A>G	rs1169099672	0.00001
NM_001242896.3(DEPDC5):c.3735C>T (p.Gly1245=)	rs758804451	0.00001
NM_001242896.3(DEPDC5):c.4359C>T (p.Ser1453=)	rs377333936	0.00001
NM_001242896.3(DEPDC5):c.1291G>A (p.Ala431Thr)	rs777844378
NM_001242896.3(DEPDC5):c.138T>C (p.Asp46=)
NM_001242896.3(DEPDC5):c.1567G>A (p.Asp523Asn)
NM_001242896.3(DEPDC5):c.2253G>A (p.Ala751=)	rs777616535
NM_001242896.3(DEPDC5):c.2850A>G (p.Pro950=)	rs1422399658
NM_001242896.3(DEPDC5):c.3177A>G (p.Ala1059=)	rs776608344
NM_001242896.3(DEPDC5):c.3600C>A (p.Leu1200=)
NM_001242896.3(DEPDC5):c.4204-6C>T	rs746382504

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