Product Details

SNP ID

rs138139624

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:42927124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCTGGCTCCCCCCTGCCGGAAGC[C/T]GGAAGCGATCTCATCGAAGGTCCGG

Phenotype

MIM: 138140 MIM: 143090

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC2A1 PubMed Links

Gene Details

Gene

SLC2A1

Gene Name

solute carrier family 2 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006516.2	1921	Missense Mutation	AGC,GGC	S466G	NP_006507.2

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