Product Details

SNP ID

rs201812504

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51993292 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTCCACATTCATTGCATATATAA[A/G]GTTTCTCCCCAGTATGAGTTCGCTG

Phenotype

MIM: 605422

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF350 PubMed Links

Gene Details

Gene

ZNF350

Gene Name

zinc finger protein 350

There are no transcripts associated with this gene.

Gene

ZNF615

Gene Name

zinc finger protein 615

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199324.1	2134	Missense Mutation	CCT,CTT	P606L	NP_001186253.1
NM_001321317.1	2134	Missense Mutation	CCT,CTT	P600L	NP_001308246.1
NM_001321318.1	2134	Missense Mutation	CCT,CTT	P602L	NP_001308247.1
NM_001321319.1	2134	Missense Mutation	CCT,CTT	P606L	NP_001308248.1
NM_001321320.1	2134	Missense Mutation	CCT,CTT	P595L	NP_001308249.1
NM_001321321.1	2134	Missense Mutation	CCT,CTT	P606L	NP_001308250.1
NM_001321322.1	2134	Missense Mutation	CCT,CTT	P602L	NP_001308251.1
NM_001321323.1	2134	Missense Mutation	CCT,CTT	P611L	NP_001308252.1
NM_198480.3	2134	Missense Mutation	CCT,CTT	P595L	NP_940882.3
XM_011526824.1	2134	Missense Mutation	CCT,CTT	P606L	XP_011525126.1
XM_011526825.1	2134	Missense Mutation	CCT,CTT	P606L	XP_011525127.1
XM_011526826.1	2134	Missense Mutation	CCT,CTT	P606L	XP_011525128.1
XM_011526829.1	2134	Missense Mutation	CCT,CTT	P487L	XP_011525131.1
XM_011526830.1	2134	Missense Mutation	CCT,CTT	P487L	XP_011525132.1
XM_017026648.1	2134	Missense Mutation	CCT,CTT	P595L	XP_016882137.1
XM_017026649.1	2134	Missense Mutation	CCT,CTT	P595L	XP_016882138.1
XM_017026650.1	2134	Missense Mutation	CCT,CTT	P487L	XP_016882139.1
XM_017026651.1	2134	Missense Mutation	CCT,CTT	P487L	XP_016882140.1

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