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GCAAAGCGTAGGCCTCACAAACATC[C/G]TGGCCGTGAAGGTAAGTTGAGCAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613324 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPATA13 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
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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SPATA13 - spermatogenesis associated 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166271.2 | 495 | Intron | NP_001159743.1 | |||
NM_001286792.1 | 495 | Missense Mutation | CCT,CGT | P,R 10 | NP_001273721.1 | |
NM_001286793.1 | 495 | Intron | NP_001273722.1 | |||
NM_001286794.1 | 495 | Intron | NP_001273723.1 | |||
NM_001286795.1 | 495 | Intron | NP_001273724.1 | |||
NM_153023.3 | 495 | Intron | NP_694568.1 |