Product Details

SNP ID
rs200687631
Assay Type
Functionally tested
NCBI dbSNP Submissions
10
Location
Chr.1:1671572 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGACATTGAAGCTGATCTCAGTG[A/G]CCGTGCACAGCGCCAGCCCGCCCAT
Phenotype
Polymorphism
A/G, Transition 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 1565 Missense Mutation GCC,GTC A215V NP_001104251.1
NM_001290264.1 1565 Missense Mutation GCC,GTC A215V NP_001277193.1
XM_011542072.1 1565 Intron XP_011540374.1

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