Product Details

SNP ID

rs201151491

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:69505943 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGCCCCGACAGCCTGGACTGTAGC[C/G]TGGACACCCTGATGGGGGACCTGCT

Phenotype

Polymorphism

C/G, 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	709	Silent Mutation	CTG,GTG	L221V	NP_056501.2
XM_011530908.2	709	Missense Mutation	CTG,GTG	L221V	XP_011529210.1
XM_011530909.2	709	Missense Mutation	CTG,GTG	L221V	XP_011529211.1

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