Product Details

SNP ID

rs149821108

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:69505958 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACTGTAGCCTGGACACCCTGATG[G/T]GGGACCTGCTGGCCGTGGTGGCCAG

Phenotype

Polymorphism

G/T, Transversion 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	724	Missense Mutation	GGG,TGG	G226W	NP_056501.2
XM_011530908.2	724	Missense Mutation	GGG,TGG	G226W	XP_011529210.1
XM_011530909.2	724	Missense Mutation	GGG,TGG	G226W	XP_011529211.1

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