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SNP ID

rs143804085

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:74764148 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGCAATAATCAGACTGAGAGCAT[A/G]TATCTTTTAACCTACAAGAGAGACC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF169 PubMed Links

Gene Details

Gene

RNF169

Gene Name

ring finger protein 169

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098638.1		Intron			NP_001092108.1
XM_011544889.2		Intron			XP_011543191.1

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