Product Details

SNP ID

rs11065157

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:120544897 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTAAATATACAACAATGGGGGATT[A/G]GTTACATTATTCTGTAAGTATGTGG

Phenotype

MIM: 615998

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF10 PubMed Links

Gene Details

Gene

RNF10

Gene Name

ring finger protein 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014868.4		Intron			NP_055683.3
XM_005254013.2		Intron			XP_005254070.1
XM_006719717.2		Intron			XP_006719780.1
XM_017020282.1		Intron			XP_016875771.1
XM_017020283.1		Intron			XP_016875772.1

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