Product Details

SNP ID
rs111033423
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:107661658 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGCAGGTCATGGCAGCGCCAGGCG[G/T]CAGGTCGGAGCCGCCGCAGCTCCCC
Phenotype
MIM: 605646
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC26A4 PubMed Links

Gene Details

Gene
SLC26A4
Gene Name
solute carrier family 26 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000441.1 20 Missense Mutation GGC,GTC G6V NP_000432.1
XM_005250425.2 20 Missense Mutation GGC,GTC G6V XP_005250482.1
XM_006716025.3 20 Missense Mutation GGC,GTC G6V XP_006716088.1
XM_017012318.1 20 Missense Mutation GGC,GTC G6V XP_016867807.1
Gene
SLC26A4-AS1
Gene Name
SLC26A4 antisense RNA 1
There are no transcripts associated with this gene.

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