Product Details

SNP ID
rs138152773
Assay Type
Functionally Tested
NCBI dbSNP Submissions
4
Location
Chr.1:54999312 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGGCACCTTCTATGCCATGGGCAG[C/T]GTCATGGTGATCGGGGGCATCATCT
Phenotype
MIM: 606412
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
BSND PubMed Links
Additional Information
For this assay, SNP(s) [rs34561376] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
BSND
Gene Name
barttin CLCNK type accessory beta subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_057176.2 369 Silent Mutation AGC,AGT S42S NP_476517.1
Gene
TMEM61
Gene Name
transmembrane protein 61
There are no transcripts associated with this gene.

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