Product Details

SNP ID

rs35780092

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:74749259 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGCGACGACGGCCAGGCCGACTCA[A/G]AGGTGCTGGGCGAGTGCGCCCGCCG

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	404	Missense Mutation	AAG,GAG	K127E	NP_001092108.1
XM_011544889.2	404	Missense Mutation	AAG,GAG	K127E	XP_011543191.1

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