Product Details

SNP ID
hCV8729307
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:16587382 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGATACAACTTTTTCCCTTAGAA[A/G]GGTATTATATCCCATTGCTACCGTT
Phenotype
MIM: 601486
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
DAZL PubMed Links

Gene Details

Gene
DAZL
Gene Name
deleted in azoospermia like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190811.1 Intron NP_001177740.1
NM_001351.3 Intron NP_001342.2

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