Product Details

SNP ID
rs9546567
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:36168769 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTGAGAAAAGAGAGTGTAGGTCAC[C/T]GAGGCCATTTGTTCTTGTAGCTCTC
Phenotype
MIM: 616066
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CCDC169-SOHLH2 PubMed Links

Gene Details

Gene
CCDC169-SOHLH2
Gene Name
CCDC169-SOHLH2 readthrough
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198910.1 2089 UTR 3 NP_001185839.1
Gene
SOHLH2
Gene Name
spermatogenesis and oogenesis specific basic helix-loop-helix 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282147.1 2089 Intron NP_001269076.1
NM_017826.2 2089 UTR 3 NP_060296.2

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