Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGTGCCTAGATATGACTTAAACCG[A/G]CACCTTGATGAAATGTGTGCTAACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613534 | ||||||||||||||||||||
Literature Links: |
FAN1 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 |
FAN1 - FANCD2/FANCI-associated nuclease 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146094.1 | 469 | Silent Mutation | CGA,CGG | R,R 58 | NP_001139566.1 | |
NM_001146095.1 | 469 | Silent Mutation | CGA,CGG | R,R 58 | NP_001139567.1 | |
NM_001146096.1 | 469 | Silent Mutation | CGA,CGG | R,R 58 | NP_001139568.1 | |
NM_014967.4 | 469 | Silent Mutation | CGA,CGG | R,R 58 | NP_055782.3 | |
XM_005254232.4 | 469 | Silent Mutation | CGA,CGG | R,R 58 | XP_005254289.1 | |
XM_005254234.4 | 469 | Silent Mutation | CGA,CGG | R,R 58 | XP_005254291.1 | |
XM_005254235.3 | 469 | Silent Mutation | CGA,CGG | R,R 58 | XP_005254292.1 | |
XM_011521370.2 | 469 | Intron | XP_011519672.1 | |||
XM_011521371.1 | 469 | UTR 5 | XP_011519673.1 | |||
XM_011521372.2 | 469 | Silent Mutation | CGA,CGG | R,R 58 | XP_011519674.1 | |
XM_017022012.1 | 469 | UTR 5 | XP_016877501.1 | |||
XM_017022013.1 | 469 | UTR 5 | XP_016877502.1 |