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TTGTAGCTATCATATCTTCGTACTC[C/T]TTATAGGCAATTGAGCCATCGGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601918 MIM: 612080 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GDF9 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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GDF9 - growth differentiation factor 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288824.2 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | NP_001275753.1 | |
NM_001288825.2 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | NP_001275754.1 | |
NM_001288826.2 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | NP_001275755.1 | |
NM_001288827.2 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | NP_001275756.1 | |
NM_001288828.2 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | NP_001275757.1 | |
XM_005271957.4 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | XP_005272014.1 | |
XM_006714585.3 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | XP_006714648.1 | |
XM_011543308.2 | 1349 | Silent Mutation | AAA,AAG | K,K 441 | XP_011541610.1 | |
XM_011543309.1 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | XP_011541611.1 | |
XM_011543310.1 | 1349 | Silent Mutation | AAA,AAG | K,K 353 | XP_011541612.1 | |
XM_011543311.2 | 1349 | Silent Mutation | AAA,AAG | K,K 263 | XP_011541613.1 |
UQCRQ - ubiquinol-cytochrome c reductase complex III subunit VII | ||||||
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There are no transcripts associated with this gene. |