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GGCCACAGCTTCAGCTGCAGAGCGA[A/G]CACTGAGGCCATTGCTAGGGGCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606371 MIM: 604643 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATF7 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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ATF7 - activating transcription factor 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130060.1 | 1483 | Missense Mutation | GCT,GTT | A,V 421 | NP_001123532.1 | |
NM_001206682.1 | 1483 | Intron | NP_001193611.1 | |||
NM_001206683.1 | 1483 | Intron | NP_001193612.1 | |||
NM_006856.2 | 1483 | Missense Mutation | GCT,GTT | A,V 442 | NP_006847.1 | |
XM_005268587.3 | 1483 | Missense Mutation | GCT,GTT | A,V 442 | XP_005268644.1 | |
XM_017018722.1 | 1483 | Missense Mutation | GCT,GTT | A,V 442 | XP_016874211.1 |
LOC100652999 - uncharacterized LOC100652999 | ||||||
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There are no transcripts associated with this gene. |
NPFF - neuropeptide FF-amide peptide precursor | ||||||
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There are no transcripts associated with this gene. |