FAAP20
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 615183
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Literature Links: |
FAAP20 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 |
| FAAP20 - Fanconi anemia core complex associated protein 20 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001146310.1 | Intron | NP_001139782.1 | ||||
| NM_001256945.1 | Intron | NP_001243874.1 | ||||
| NM_001256946.1 | Intron | NP_001243875.1 | ||||
| NM_001256947.1 | Intron | NP_001243876.1 | ||||
| NM_001282670.1 | Intron | NP_001269599.1 | ||||
| NM_001282671.1 | Intron | NP_001269600.1 | ||||
| NM_001282672.1 | Intron | NP_001269601.1 | ||||
| NM_001282673.1 | Intron | NP_001269602.1 | ||||
| NM_182533.2 | Intron | NP_872339.2 | ||||
| XM_006710419.3 | Intron | XP_006710482.1 | ||||
| XM_006710421.3 | Intron | XP_006710484.1 | ||||
| XM_011540914.2 | Intron | XP_011539216.1 | ||||
| XM_011540921.2 | Intron | XP_011539223.1 | ||||
| XM_011540922.1 | Intron | XP_011539224.1 | ||||
| XM_017000553.1 | Intron | XP_016856042.1 | ||||
| XM_017000554.1 | Intron | XP_016856043.1 | ||||
| XM_017000555.1 | Intron | XP_016856044.1 | ||||
| XM_017000556.1 | Intron | XP_016856045.1 | ||||
| XM_017000557.1 | Intron | XP_016856046.1 | ||||
| LOC105378592 - uncharacterized LOC105378592 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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