Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608111 MIM: 602169 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FANCL 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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FANCL - Fanconi anemia complementation group L | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114636.1 | 1093 | Silent Mutation | TCC,TCT | S,S 332 | NP_001108108.1 | |
NM_018062.3 | 1093 | Silent Mutation | TCC,TCT | S,S 327 | NP_060532.2 | |
XM_005264395.3 | 1093 | Silent Mutation | TCC,TCT | S,S 327 | XP_005264452.1 | |
XM_005264397.4 | 1093 | Silent Mutation | TCC,TCT | S,S 210 | XP_005264454.1 | |
XM_011532939.2 | 1093 | Silent Mutation | TCC,TCT | S,S 347 | XP_011531241.1 | |
XM_011532940.2 | 1093 | Silent Mutation | TCC,TCT | S,S 342 | XP_011531242.1 | |
XM_011532941.1 | 1093 | Silent Mutation | TCC,TCT | S,S 347 | XP_011531243.1 | |
XM_011532942.2 | 1093 | Silent Mutation | TCC,TCT | S,S 332 | XP_011531244.1 | |
XM_011532944.2 | 1093 | Silent Mutation | TCC,TCT | S,S 230 | XP_011531246.1 | |
XM_011532945.2 | 1093 | Silent Mutation | TCC,TCT | S,S 215 | XP_011531247.1 | |
XM_017004414.1 | 1093 | Silent Mutation | TCC,TCT | S,S 342 | XP_016859903.1 | |
XM_017004415.1 | 1093 | Intron | XP_016859904.1 | |||
XM_017004416.1 | 1093 | Silent Mutation | TCC,TCT | S,S 210 | XP_016859905.1 |
Set Membership: |
HapMap Validated |