Product Details

SNP ID
rs12821572
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:12358826 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATAGCAGGAAAGATTTCTGGCATG[A/G]CTTTTGTAAAATGTTAGGTAAATTA
Phenotype
MIM: 616598
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BORCS5 PubMed Links

Gene Details

Gene
BORCS5
Gene Name
BLOC-1 related complex subunit 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_011520551.2 Intron XP_011518853.1
XM_011520552.2 Intron XP_011518854.1
XM_011520553.2 Intron XP_011518855.1
XM_017018778.1 Intron XP_016874267.1
Gene
LOH12CR2
Gene Name
loss of heterozygosity, 12, chromosomal region 2 (non-protein coding)
There are no transcripts associated with this gene.

Gene
MANSC1
Gene Name
MANSC domain containing 1
There are no transcripts associated with this gene.

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