Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605430 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPAG9 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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SPAG9 - sperm associated antigen 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130527.2 | 4207 | Missense Mutation | AAT,AGT | N,S 1310 | NP_001123999.1 | |
NM_001130528.2 | 4207 | Missense Mutation | AAT,AGT | N,S 1320 | NP_001124000.1 | |
NM_001251971.1 | 4207 | Missense Mutation | AAT,AGT | N,S 1176 | NP_001238900.1 | |
NM_003971.5 | 4207 | Missense Mutation | AAT,AGT | N,S 1306 | NP_003962.3 | |
XM_005257768.2 | 4207 | Missense Mutation | AAT,AGT | N,S 1333 | XP_005257825.1 | |
XM_005257771.2 | 4207 | Missense Mutation | AAT,AGT | N,S 1319 | XP_005257828.1 | |
XM_005257774.3 | 4207 | Missense Mutation | AAT,AGT | N,S 1163 | XP_005257831.1 | |
XM_017025283.1 | 4207 | Missense Mutation | AAT,AGT | N,S 1190 | XP_016880772.1 | |
XM_017025284.1 | 4207 | Missense Mutation | AAT,AGT | N,S 1177 | XP_016880773.1 | |
XM_017025285.1 | 4207 | Missense Mutation | AAT,AGT | N,S 1168 | XP_016880774.1 |
Set Membership: |
HapMap |