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ATTTAAGAGCATCGAACAATAATAA[A/G]TGTTTGATTAAATAAAAACCGTGAC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613897 MIM: 602835 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FANCF 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)
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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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FANCF - Fanconi anemia complementation group F | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022725.3 | 429 | Intron | NP_073562.1 |
GAS2 - growth arrest specific 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143830.1 | 429 | Intron | NP_001137302.1 | |||
NM_005256.3 | 429 | Intron | NP_005247.1 | |||
NM_177553.2 | 429 | Intron | NP_808221.1 | |||
XM_011519971.2 | 429 | Intron | XP_011518273.1 | |||
XM_011519972.2 | 429 | UTR 5 | XP_011518274.1 | |||
XM_011519975.1 | 429 | Intron | XP_011518277.1 | |||
XM_011519978.2 | 429 | Intron | XP_011518280.1 | |||
XM_017017528.1 | 429 | Intron | XP_016873017.1 | |||
XM_017017529.1 | 429 | Intron | XP_016873018.1 | |||
XM_017017530.1 | 429 | Intron | XP_016873019.1 | |||
XM_017017531.1 | 429 | Intron | XP_016873020.1 | |||
XM_017017532.1 | 429 | Intron | XP_016873021.1 |