Product Details

SNP ID
rs139595449
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:117955323 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATCCTTCCTTTATAGCCTTCAGC[G/T]TATGTATTAGAGATTTTTAAAGGGA
Phenotype
MIM: 616554 MIM: 604737
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SPAG17 PubMed Links

Gene Details

Gene
SPAG17
Gene Name
sperm associated antigen 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_206996.2 2484 Intron NP_996879.1
XM_006710426.3 2484 Intron XP_006710489.1
XM_006710427.3 2484 Intron XP_006710490.1
XM_006710428.3 2484 Intron XP_006710491.1
XM_006710429.3 2484 Intron XP_006710492.1
XM_006710431.3 2484 Intron XP_006710494.1
XM_011540934.1 2484 Intron XP_011539236.1
XM_011540935.2 2484 Intron XP_011539237.1
XM_011540936.2 2484 Intron XP_011539238.1
XM_011540937.2 2484 Intron XP_011539239.1
XM_011540939.2 2484 Intron XP_011539241.1
XM_011540941.2 2484 Intron XP_011539243.1
XM_011540942.2 2484 Intron XP_011539244.1
Gene
WDR3
Gene Name
WD repeat domain 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006784.2 2484 Silent Mutation GCG,GCT A806A NP_006775.1

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