Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCTTCTTGCCCAGCTGGGCGGCCC[A/G]GTGCTCCCGCAGCTCACTTGCCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 164012 MIM: 602327 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFKB2 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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NFKB2 - nuclear factor kappa B subunit 2 | ||||||
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There are no transcripts associated with this gene. |
PSD - pleckstrin and Sec7 domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270965.1 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | NP_001257894.1 | |
NM_001270966.1 | 2973 | Missense Mutation | CGG,TGG | R,W 543 | NP_001257895.1 | |
NM_002779.4 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | NP_002770.3 | |
XM_011539968.1 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | XP_011538270.1 | |
XM_011539969.2 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | XP_011538271.1 | |
XM_017016433.1 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | XP_016871922.1 | |
XM_017016434.1 | 2973 | Missense Mutation | CGG,TGG | R,W 922 | XP_016871923.1 |