Product Details

SNP ID

rs147875150

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:69505758 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAATCTTTGCAGAGACTTTTCGAAC[C/T]GACTACTCCGGCCCCCCCTCTGCGG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM155B PubMed Links

Gene Details

Gene

FAM155B

Gene Name

family with sequence similarity 155 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015686.2	524	Missense Mutation	CCG,CTG	P159L	NP_056501.2
XM_011530908.2	524	Missense Mutation	CCG,CTG	P159L	XP_011529210.1
XM_011530909.2	524	Missense Mutation	CCG,CTG	P159L	XP_011529211.1

View Full Product Details