Product Details

SNP ID

rs148348449

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:117241742 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTCCGCTGGCTGCAGGAGAGCCGC[C/T]GCTCGCGGAAGCTCATCCTGTTCAT

Phenotype

MIM: 193001

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC18A2 PubMed Links

Gene Details

Gene

SLC18A2

Gene Name

solute carrier family 18 member A2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003054.4	212	Missense Mutation	CGC,TGC	R17C	NP_003045.2

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