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GCCATTAGATATTCGGGAGTGCTGG[C/T]AAGCAACTGCTTTATTTCATAATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613645 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATF7IP2 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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ATF7IP2 - activating transcription factor 7 interacting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256160.1 | Intron | NP_001243089.1 | ||||
NM_024997.3 | Intron | NP_079273.2 | ||||
XM_006720953.3 | Intron | XP_006721016.1 | ||||
XM_006720954.3 | Intron | XP_006721017.1 | ||||
XM_011522666.2 | Intron | XP_011520968.1 | ||||
XM_017023705.1 | Intron | XP_016879194.1 | ||||
XM_017023706.1 | Intron | XP_016879195.1 | ||||
XM_017023707.1 | Intron | XP_016879196.1 | ||||
XM_017023708.1 | Intron | XP_016879197.1 | ||||
XM_017023709.1 | Intron | XP_016879198.1 | ||||
XM_017023710.1 | Intron | XP_016879199.1 | ||||
XM_017023711.1 | Intron | XP_016879200.1 |