Product Details

SNP ID
rs142955756
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75093751 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCACGTGTATCGGCATCTTCTTC[A/T]CTGAATTGCAATGGGAGTTCCAGGC
Phenotype
MIM: 603879
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC16A5 PubMed Links

Gene Details

Gene
SLC16A5
Gene Name
solute carrier family 16 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271765.1 363 Missense Mutation ACT,TCT T39S NP_001258694.1
NM_004695.3 363 Missense Mutation ACT,TCT T39S NP_004686.1
XM_005257790.1 363 Missense Mutation ACT,TCT T79S XP_005257847.1
XM_011525462.1 363 Missense Mutation ACT,TCT T79S XP_011523764.1
XM_017025293.1 363 UTR 5 XP_016880782.1

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