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Search Thermo Fisher Scientific
ACTGACTCCATTGGATGTGCTGACC[A/G]AACTATGCTGTATAGCTTCTGTATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 123811 | ||||||||||||||||||||
Literature Links: |
ATF2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ATF2 - activating transcription factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256090.1 | 1601 | Missense Mutation | TCG,TTG | S,L 456 | NP_001243019.1 | |
NM_001256091.1 | 1601 | Missense Mutation | TCG,TTG | S,L 438 | NP_001243020.1 | |
NM_001256092.1 | 1601 | Missense Mutation | TCG,TTG | S,L 398 | NP_001243021.1 | |
NM_001256093.1 | 1601 | UTR 3 | NP_001243022.1 | |||
NM_001256094.1 | 1601 | Intron | NP_001243023.1 | |||
NM_001880.3 | 1601 | Missense Mutation | TCG,TTG | S,L 456 | NP_001871.2 |