Product Details

SNP ID
rs114985669
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:181892173 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAAGTGCCGCAGCTCCTGGCAAG[C/G]GTCGGAGACGGAGGATCTGTCCACA
Phenotype
MIM: 118990
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SSFA2 PubMed Links

Gene Details

Gene
SSFA2
Gene Name
sperm specific antigen 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130445.2 366 Missense Mutation GCG,GGG A36G NP_001123917.1
NM_001287503.1 366 Missense Mutation GCG,GGG A36G NP_001274432.1
NM_001287504.1 366 UTR 5 NP_001274433.1
NM_001287505.1 366 Missense Mutation GCG,GGG A36G NP_001274434.1
NM_006751.6 366 Missense Mutation GCG,GGG A36G NP_006742.2
XM_005246812.1 366 Missense Mutation GCG,GGG A36G XP_005246869.1
XM_005246813.1 366 Missense Mutation GCG,GGG A36G XP_005246870.1
XM_011511701.2 366 Missense Mutation GCG,GGG A36G XP_011510003.1
XM_011511702.2 366 Intron XP_011510004.1
XM_011511703.2 366 Intron XP_011510005.1
XM_017004782.1 366 Missense Mutation GCG,GGG A36G XP_016860271.1

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