Product Details

SNP ID
rs36000446
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7041808 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGGCTGGACCACAGGAGGGCAG[C/T]GCCCTGGGCAACCCTATGTAGATGA
Phenotype
MIM: 615765
Polymorphism
C/T, Transition 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 1858 Silent Mutation GCA,GCG A429A NP_699188.1
XM_005256488.3 1858 Silent Mutation GCA,GCG A524A XP_005256545.2
XM_017024281.1 1858 Intron XP_016879770.1
XM_017024282.1 1858 Silent Mutation GCA,GCG A268A 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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