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TTATTGCATCCCCAGGCATCTAATT[A/G]TGTGACATATGATGCCAAAGAAAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609868 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPATA7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
SPATA7 - spermatogenesis associated 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040428.3 | 1266 | Missense Mutation | TAT,TGT | Y,C 276 | NP_001035518.1 | |
NM_018418.4 | 1266 | Missense Mutation | TAT,TGT | Y,C 308 | NP_060888.2 | |
XM_005267851.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 309 | XP_005267908.1 | |
XM_005267852.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 277 | XP_005267909.1 | |
XM_005267854.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 245 | XP_005267911.1 | |
XM_005267855.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 245 | XP_005267912.1 | |
XM_006720204.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 309 | XP_006720267.1 | |
XM_006720205.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 309 | XP_006720268.1 | |
XM_011536951.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 258 | XP_011535253.1 | |
XM_011536952.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 252 | XP_011535254.1 | |
XM_011536953.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 203 | XP_011535255.1 | |
XM_017021452.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 257 | XP_016876941.1 | |
XM_017021453.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 245 | XP_016876942.1 | |
XM_017021454.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 244 | XP_016876943.1 | |
XM_017021455.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 244 | XP_016876944.1 | |
XM_017021456.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 244 | XP_016876945.1 | |
XM_017021457.1 | 1266 | Missense Mutation | TAT,TGT | Y,C 202 | XP_016876946.1 |