Product Details

SNP ID

rs113123140

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:72056116 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTACAGTACTGACCAGGTTCTG[C/T]CTGGCAGGTTCCCAGGTCTAAAAGA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C9orf57 PubMed Links

Gene Details

Gene

C9orf57

Gene Name

chromosome 9 open reading frame 57

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128618.1	244	Missense Mutation	ACA,GCA	T102A	NP_001122090.1
XM_011518225.2	244	Missense Mutation	ACA,GCA	T52A	XP_011516527.1

View Full Product Details