Product Details

SNP ID
rs74045224
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:36168468 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCACACATCAATTTATTCATTAGT[A/T]GTCAAGTGAGGAGGTAAACCCCTCT
Phenotype
MIM: 616066
Polymorphism
A/T, Transversion 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 2390 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 2390 Intron NP_001269076.1
NM_017826.2 2390 UTR 3 NP_060296.2

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