Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAAACTCTGCCACACACAACATAA[C/T]GATCTTTAGGACAGTTACCACTTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300515 | ||||||||||||||||||||
Literature Links: |
FANCB 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 |
FANCB - Fanconi anemia complementation group B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001018113.2 | 2191 | Missense Mutation | NP_001018123.1 | |||
NM_001324162.1 | 2191 | Missense Mutation | NP_001311091.1 | |||
NM_152633.3 | 2191 | Missense Mutation | NP_689846.1 | |||
XM_011545470.2 | 2191 | Missense Mutation | XP_011543772.1 | |||
XM_017029355.1 | 2191 | Missense Mutation | XP_016884844.1 | |||
XM_017029356.1 | 2191 | Missense Mutation | XP_016884845.1 |