Product Details

SNP ID
rs200001492
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:128794255 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTGATCGCTGATGGTCTCGATGAT[A/G]GTCATATTTCACAGAAATAATGAGG
Phenotype
MIM: 615806
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC15A4 PubMed Links

Gene Details

Gene
SLC15A4
Gene Name
solute carrier family 15 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145648.3 1848 Missense Mutation CAT,TAT H559Y NP_663623.1
XM_011537895.1 1848 Missense Mutation CAT,TAT H609Y XP_011536197.1
XM_017018791.1 1848 Intron XP_016874280.1
XM_017018792.1 1848 Intron XP_016874281.1
XM_017018793.1 1848 Intron XP_016874282.1

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