Product Details

SNP ID
rs191550854
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:117954033 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGAGGATTATGGAGGCTATTGA[A/G]TTGTACCGAGAAGAAACTGCAAAAA
Phenotype
MIM: 616554 MIM: 604737
Polymorphism
A/G, Transition 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 3887 UTR 3 NP_996879.1
XM_006710426.3 3887 UTR 3 XP_006710489.1
XM_006710427.3 3887 UTR 3 XP_006710490.1
XM_006710428.3 3887 UTR 3 XP_006710491.1
XM_006710429.3 3887 UTR 3 XP_006710492.1
XM_006710431.3 3887 UTR 3 XP_006710494.1
XM_011540934.1 3887 UTR 3 XP_011539236.1
XM_011540935.2 3887 UTR 3 XP_011539237.1
XM_011540936.2 3887 UTR 3 XP_011539238.1
XM_011540937.2 3887 UTR 3 XP_011539239.1
XM_011540939.2 3887 UTR 3 XP_011539241.1
XM_011540941.2 3887 UTR 3 XP_011539243.1
XM_011540942.2 3887 UTR 3 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 3887 Silent Mutation GAA,GAG E765E NP_006775.1

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