Product Details

SNP ID

rs201365142

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:102326672 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTGAAAAGTCATATATAGGGAAG[C/G]GGGGACTGGCCCGACATTTTAAACT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ZNF839 PubMed Links

Gene Details

Gene

ZNF839

Gene Name

zinc finger protein 839

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001267827.1	991	Missense Mutation	CGG,GGG	R210G	NP_001254756.1
NM_001267828.1	991	Missense Mutation	CGG,GGG	R210G	NP_001254757.1
NM_018335.4	991	Missense Mutation	CGG,GGG	R326G	NP_060805.3
XM_006720203.3	991	Missense Mutation	CGG,GGG	R238G	XP_006720266.2
XM_011536945.1	991	Missense Mutation	CGG,GGG	R360G	XP_011535247.1
XM_011536946.2	991	Missense Mutation	CGG,GGG	R360G	XP_011535248.1
XM_011536948.2	991	Missense Mutation	CGG,GGG	R210G	XP_011535250.1
XM_011536949.2	991	Missense Mutation	CGG,GGG	R360G	XP_011535251.1
XM_011536950.2	991	Missense Mutation	CGG,GGG	R360G	XP_011535252.1
XM_017021447.1	991	Missense Mutation	CGG,GGG	R326G	XP_016876936.1
XM_017021448.1	991	Missense Mutation	CGG,GGG	R326G	XP_016876937.1
XM_017021449.1	991	Intron			XP_016876938.1
XM_017021450.1	991	Missense Mutation	CGG,GGG	R256G	XP_016876939.1
XM_017021451.1	991	Missense Mutation	CGG,GGG	R210G	XP_016876940.1

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