Product Details

SNP ID

rs4648793

Assay Type

Functionally tested

NCBI dbSNP Submissions

28

Location

Chr.1:1740343 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGCTACTTTCTTTTTTTTTGAGA[C/T]GGGAGTCTCGCTGTGTCGCCTAGCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC35E2 PubMed Links

Gene Details

Gene

SLC35E2

Gene Name

solute carrier family 35 member E2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199787.1		Intron			NP_001186716.1
NM_182838.2		Intron			NP_878258.1

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