Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600185 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BRCA2 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) - Not Available | |||
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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BRCA2 - BRCA2, DNA repair associated | ||||||
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There are no transcripts associated with this gene. |
N4BP2L1 - NEDD4 binding protein 2 like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079691.1 | 879 | UTR 3 | NP_001073159.1 | |||
NM_001286459.1 | 879 | UTR 3 | NP_001273388.1 | |||
NM_001286460.1 | 879 | Missense Mutation | AAT,ATT | N,I 178 | NP_001273389.1 | |
NM_001286461.1 | 879 | Missense Mutation | ATG,TTG | M,L 181 | NP_001273390.1 | |
NM_052818.2 | 879 | UTR 3 | NP_438169.2 | |||
XM_006719890.3 | 879 | UTR 3 | XP_006719953.1 | |||
XM_011535301.2 | 879 | UTR 3 | XP_011533603.1 | |||
XM_011535302.2 | 879 | UTR 3 | XP_011533604.1 | |||
XM_011535303.2 | 879 | Intron | XP_011533605.1 | |||
XM_011535304.2 | 879 | UTR 3 | XP_011533606.1 | |||
XM_017020836.1 | 879 | UTR 3 | XP_016876325.1 | |||
XM_017020837.1 | 879 | UTR 3 | XP_016876326.1 | |||
XM_017020838.1 | 879 | UTR 3 | XP_016876327.1 | |||
XM_017020839.1 | 879 | Intron | XP_016876328.1 | |||
XM_017020840.1 | 879 | UTR 3 | XP_016876329.1 | |||
XM_017020841.1 | 879 | UTR 3 | XP_016876330.1 | |||
XM_017020842.1 | 879 | UTR 3 | XP_016876331.1 |