Product Details
- SNP ID
-
rs148354979
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:50966281 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTGTTTCCCATGGGCTCACTCATT[A/G]CCATACATCACTTGCCACACTATCA
- Phenotype
-
MIM: 605430
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SPAG9
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs9896965] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- SPAG9
- Gene Name
- sperm associated antigen 9
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001130527.2 |
4205 |
Silent Mutation |
GGC,GGT |
G1309G |
NP_001123999.1 |
NM_001130528.2 |
4205 |
Silent Mutation |
GGC,GGT |
G1319G |
NP_001124000.1 |
NM_001251971.1 |
4205 |
Silent Mutation |
GGC,GGT |
G1175G |
NP_001238900.1 |
NM_003971.5 |
4205 |
Silent Mutation |
GGC,GGT |
G1305G |
NP_003962.3 |
XM_005257768.2 |
4205 |
Silent Mutation |
GGC,GGT |
G1332G |
XP_005257825.1 |
XM_005257771.2 |
4205 |
Silent Mutation |
GGC,GGT |
G1318G |
XP_005257828.1 |
XM_005257774.3 |
4205 |
Silent Mutation |
GGC,GGT |
G1162G |
XP_005257831.1 |
XM_017025283.1 |
4205 |
Silent Mutation |
GGC,GGT |
G1189G |
XP_016880772.1 |
XM_017025284.1 |
4205 |
Silent Mutation |
GGC,GGT |
G1176G |
XP_016880773.1 |
XM_017025285.1 |
4205 |
Silent Mutation |
GGC,GGT |
G1167G |
XP_016880774.1 |
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