Product Details

SNP ID

rs200881069

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:157162598 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCTTAGCCACGATATCTACCTCT[C/T]TGTCATGTGATGTGACCCTTGTTTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM71B PubMed Links

Gene Details

Gene

FAM71B

Gene Name

family with sequence similarity 71 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130899.2	1767	Missense Mutation	AAA,AGA	K556R	NP_570969.2

View Full Product Details