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TTGTTTTTGACGTCCTGATTCGTTT[C/T]GCTTTTGGCTTTCCCAGAGTTTCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 610853 | ||||||||||||||||||||
Literature Links: |
AHCTF1 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 |
AHCTF1 - AT-hook containing transcription factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323342.1 | 6978 | Silent Mutation | GCA,GCG | A,A 2190 | NP_001310271.1 | |
NM_001323343.1 | 6978 | Silent Mutation | GCA,GCG | A,A 2190 | NP_001310272.1 | |
NM_015446.4 | 6978 | Intron | NP_056261.4 | |||
XM_006711758.1 | 6978 | Intron | XP_006711821.1 | |||
XM_011544156.2 | 6978 | Intron | XP_011542458.2 | |||
XM_011544157.2 | 6978 | Intron | XP_011542459.2 |