Product Details

SNP ID
rs191024007
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:181892217 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCACAGAAGCGACGACGCAGGAC[A/G]AGGAGGAGGACGAGGAGGAGGACCT
Phenotype
MIM: 118990
Polymorphism
A/G, Transition 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_001130445.2 410 Missense Mutation AAG,GAG K51E NP_001123917.1
NM_001287503.1 410 Missense Mutation AAG,GAG K51E NP_001274432.1
NM_001287504.1 410 UTR 5 NP_001274433.1
NM_001287505.1 410 Missense Mutation AAG,GAG K51E NP_001274434.1
NM_006751.6 410 Missense Mutation AAG,GAG K51E NP_006742.2
XM_005246812.1 410 Missense Mutation AAG,GAG K51E XP_005246869.1
XM_005246813.1 410 Missense Mutation AAG,GAG K51E XP_005246870.1
XM_011511701.2 410 Missense Mutation AAG,GAG K51E XP_011510003.1
XM_011511702.2 410 Intron XP_011510004.1
XM_011511703.2 410 Intron XP_011510005.1
XM_017004782.1 410 Missense Mutation AAG,GAG K51E XP_016860271.1

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