Product Details

SNP ID
rs191656427
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7042355 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCACCACCAGCGCTGCTCCGTAT[A/C]CCCCCAGGCCCCGGTCTAAAGCGTG
Phenotype
MIM: 615765
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC16A11 PubMed Links

Gene Details

Gene
SLC16A11
Gene Name
solute carrier family 16 member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153357.1 1398 Missense Mutation GGA,GTA G276V NP_699188.1
XM_005256488.3 1398 Missense Mutation GGA,GTA G371V XP_005256545.2
XM_017024281.1 1398 Missense Mutation GGA,GTA G371V XP_016879770.1
XM_017024282.1 1398 Intron XP_016879771.1
Gene
SLC16A13
Gene Name
solute carrier family 16 member 13
There are no transcripts associated with this gene.

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