List of variants in gene ZNF407 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_017757.3(ZNF407):c.33T>C (p.Asp11=)	rs7243081	0.99326
NM_017757.3(ZNF407):c.6444G>A (p.Thr2148=)	rs3744913	0.76676
NM_017757.3(ZNF407):c.1248T>C (p.Pro416=)	rs3794941	0.19620
NM_017757.3(ZNF407):c.1578G>A (p.Thr526=)	rs7227391	0.11528
NM_017757.3(ZNF407):c.1534G>A (p.Gly512Arg)	rs7227263	0.11518
NM_017757.3(ZNF407):c.1263C>T (p.Leu421=)	rs17817969	0.11505
NM_017757.3(ZNF407):c.206A>G (p.Asn69Ser)	rs3794942	0.07157
NM_017757.3(ZNF407):c.181A>G (p.Ser61Gly)	rs75994611	0.01776
NM_017757.3(ZNF407):c.1077A>G (p.Val359=)	rs77148611	0.01062
NM_017757.3(ZNF407):c.6007G>A (p.Glu2003Lys)	rs150419019	0.00602
NM_017757.3(ZNF407):c.6384G>A (p.Ala2128=)	rs138221111	0.00335
NM_017757.3(ZNF407):c.490A>G (p.Arg164Gly)	rs74861823	0.00314
NM_017757.3(ZNF407):c.1116T>C (p.Ala372=)	rs147229491	0.00312
NM_017757.3(ZNF407):c.6069G>T (p.Leu2023=)	rs189911859	0.00252
NM_017757.3(ZNF407):c.1908C>T (p.Thr636=)	rs187139901	0.00248
NM_017757.3(ZNF407):c.4278G>A (p.Leu1426=)	rs201719725	0.00231
NM_017757.3(ZNF407):c.1927T>C (p.Leu643=)	rs139800364	0.00140
NM_017757.3(ZNF407):c.3717C>T (p.Asp1239=)	rs201823505	0.00029
NM_017757.3(ZNF407):c.4010A>G (p.Tyr1337Cys)	rs760492866	0.00020
NM_017757.3(ZNF407):c.4146G>A (p.Thr1382=)	rs373279175	0.00019
NM_017757.3(ZNF407):c.3974C>G (p.Pro1325Arg)	rs368198591	0.00016
NM_017757.3(ZNF407):c.1184T>G (p.Leu395Trp)	rs201998501	0.00011
NM_017757.3(ZNF407):c.1446G>A (p.Ala482=)	rs368834630	0.00006
NM_017757.3(ZNF407):c.246G>A (p.Glu82=)	rs748374834	0.00003
NM_017757.3(ZNF407):c.3902C>T (p.Pro1301Leu)	rs750218080	0.00003
NM_017757.3(ZNF407):c.3675G>A (p.Glu1225=)	rs200667048	0.00002
NM_017757.3(ZNF407):c.1258A>G (p.Ile420Val)	rs587780522	0.00001
NM_017757.3(ZNF407):c.5701C>T (p.Arg1901Trp)	rs769492762	0.00001
NM_017757.3(ZNF407):c.4507T>C (p.Leu1503=)	rs12327359
NM_017757.3(ZNF407):c.5085C>G (p.Gly1695=)	rs34940122
NM_017757.3(ZNF407):c.615T>C (p.Ala205=)	rs1305024488

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