Product Details

SNP ID
rs34994431
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7041898 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCGGTGAAGTCTCCTGTCTCATC[C/T]CTTAGGAAGCCTGAGGAGATGGGTA
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 1768 Silent Mutation AGA,AGG R399R NP_699188.1
XM_005256488.3 1768 Silent Mutation AGA,AGG R494R XP_005256545.2
XM_017024281.1 1768 UTR 3 XP_016879770.1
XM_017024282.1 1768 Silent Mutation AGA,AGG R238R 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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