Product Details

SNP ID

rs200504139

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:69505787 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACTCCGGCCCCCCCTCTGCGGCCC[C/T]CTGACTCCCTTTCCCGTGCCCCGGC

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	553	Missense Mutation	CCT,TCT	P169S	NP_056501.2
XM_011530908.2	553	Missense Mutation	CCT,TCT	P169S	XP_011529210.1
XM_011530909.2	553	Missense Mutation	CCT,TCT	P169S	XP_011529211.1

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