Product Details

SNP ID

rs138944821

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:1201678 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGAGGCTCGTGCTGCCCAACCCC[A/G]GCCTAGACGCCCGGATCCCGTCCCT

Phenotype

MIM: 608893

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC6A19 PubMed Links

Gene Details

Gene

SLC6A19

Gene Name

solute carrier family 6 member 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003841.2	84	Missense Mutation	AGC,GGC	S10G	NP_001003841.1

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