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TTTCCCATTTTCAGGACCCTCCGAT[A/G]TGTTCCAGAGGAATCCAAAGACAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MIER3 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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MIER3 - MIER family member 3 | ||||||
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There are no transcripts associated with this gene. |
SETD9 - SET domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171990.2 | 510 | Missense Mutation | TAT,TGT | Y,C 37 | NP_001165461.1 | |
NM_001323018.1 | 510 | Missense Mutation | TAT,TGT | Y,C 11 | NP_001309947.1 | |
NM_001323019.1 | 510 | Missense Mutation | TAT,TGT | Y,C 37 | NP_001309948.1 | |
NM_001323020.1 | 510 | Missense Mutation | TAT,TGT | Y,C 11 | NP_001309949.1 | |
NM_001323022.1 | 510 | Intron | NP_001309951.1 | |||
NM_153706.3 | 510 | Missense Mutation | TAT,TGT | Y,C 37 | NP_714917.2 | |
XM_005248426.4 | 510 | Intron | XP_005248483.1 | |||
XM_011543139.2 | 510 | Missense Mutation | TAT,TGT | Y,C 5 | XP_011541441.1 | |
XM_011543140.2 | 510 | UTR 5 | XP_011541442.1 |