Product Details

SNP ID
rs150967302
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:134899367 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGATCATCTGCATAAAATATGAGCT[C/T]CGTGGGGAACACGAAAACAGGAAGA
Phenotype
MIM: 300674
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MOSPD1 PubMed Links

Gene Details

Gene
MOSPD1
Gene Name
motile sperm domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001306188.1 524 Missense Mutation AAG,GAG K23E NP_001293117.1
NM_019556.2 524 Missense Mutation AAG,GAG K23E NP_062456.1
XM_011531366.2 524 Missense Mutation AAG,GAG K23E XP_011529668.1
XM_017029653.1 524 Missense Mutation AAG,GAG K23E XP_016885142.1
XM_017029654.1 524 Missense Mutation AAG,GAG K23E XP_016885143.1

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