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CCGGCGTGAACTTCAGCGAGTTCAC[A/G]GGTGTGTGGAAGTACATCACGGACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606517 MIM: 601057 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AHRR 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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AHRR - aryl-hydrocarbon receptor repressor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242412.1 | 358 | Intron | NP_001229341.1 | |||
NM_020731.4 | 358 | Intron | NP_065782.2 |
PDCD6 - programmed cell death 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267556.1 | 358 | Silent Mutation | ACA,ACG | T,T 86 | NP_001254485.1 | |
NM_001267557.1 | 358 | Intron | NP_001254486.1 | |||
NM_001267558.1 | 358 | Silent Mutation | ACA,ACG | T,T 16 | NP_001254487.1 | |
NM_001267559.1 | 358 | Intron | NP_001254488.1 | |||
NM_013232.3 | 358 | Silent Mutation | ACA,ACG | T,T 86 | NP_037364.1 |