Product Details

SNP ID

rs76803829

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:36170783 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGCATTCTCTGAGGCGGAGCTTGA[C/T]GGAACTTTAATGAGAAAGAAAACAA

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	1551	Silent Mutation	CCA,CCG	P412P	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	1551	Intron			NP_001269076.1
NM_017826.2	1551	Silent Mutation	CCA,CCG	P335P	NP_060296.2

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