Product Details

SNP ID

rs17616564

Assay Type

Functionally tested

NCBI dbSNP Submissions

44

Location

Chr.1:108565773 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAGCGGAAAGGATTTCTTTCTTTT[A/G]GCCAGAGTACATCCTTCTGTTTTCA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM102B PubMed Links

Gene Details

Gene

FAM102B

Gene Name

family with sequence similarity 102 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010883.2		Intron			NP_001010883.2

View Full Product Details