Product Details

SNP ID

rs10065641

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:179919646 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGACTTAAACACTTGTCACTTTA[C/T]GTCATGCTCAACACGGAGGCTGGAA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF130 PubMed Links

Gene Details

Gene

RNF130

Gene Name

ring finger protein 130

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001280801.1	2359	Intron			NP_001267730.1
NM_018434.5	2359	Intron			NP_060904.2
XM_011534593.2	2359	UTR 3			XP_011532895.1

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