Product Details

SNP ID

rs4648609

Assay Type

Validated

NCBI dbSNP Submissions

43

Location

Chr.1:1671097 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

ATCCTTCCTGCCATCGTGACACCAG[G/C]ACACAGATGGCCACAAGGAAGCAGA

Phenotype

Polymorphism

G/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC35E2B PubMed Links

Gene Details

Gene

SLC35E2B

Gene Name

solute carrier family 35 member E2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001110781.2		Intron			NP_001104251.1
NM_001290264.1		Intron			NP_001277193.1
XM_011542072.1		Intron			XP_011540374.1

View Full Product Details