Product Details

SNP ID

rs1064512

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:64989752 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGGGACGCGCACGGCGTTGCGCG[C/G]GCTTCCTGCGGCGCCAAGCGCTGGT

Phenotype

MIM: 600229

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SLC1A4 PubMed Links

Gene Details

Gene

SLC1A4

Gene Name

solute carrier family 1 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193493.1	392	Intron			NP_001180422.1
NM_003038.4	392	Missense Mutation	CGC,GGC	R37G	NP_003029.2
XM_006712079.2	392	Intron			XP_006712142.1

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