Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTGACCCGAAGCAGCGCTGCATA[G/T]GTGCTGTAGCGGGATTTCTGAGGCA
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 |
---|---|---|
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 |
NFKB2 - nuclear factor kappa B subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077494.3 | 3071 | Intron | NP_001070962.1 | |||
NM_001261403.2 | 3071 | Intron | NP_001248332.1 | |||
NM_001288724.1 | 3071 | Intron | NP_001275653.1 | |||
NM_001322934.1 | 3071 | Intron | NP_001309863.1 | |||
NM_001322935.1 | 3071 | Intron | NP_001309864.1 | |||
NM_002502.5 | 3071 | Intron | NP_002493.3 | |||
XM_011539830.2 | 3071 | Intron | XP_011538132.1 | |||
XM_011539831.2 | 3071 | Intron | XP_011538133.1 | |||
XM_017016278.1 | 3071 | Intron | XP_016871767.1 |
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 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | NP_001257894.1 | |
NM_001270966.1 | 3071 | Silent Mutation | ACA,ACC | T,T 575 | NP_001257895.1 | |
NM_002779.4 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | NP_002770.3 | |
XM_011539968.1 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | XP_011538270.1 | |
XM_011539969.2 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | XP_011538271.1 | |
XM_017016433.1 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | XP_016871922.1 | |
XM_017016434.1 | 3071 | Silent Mutation | ACA,ACC | T,T 954 | XP_016871923.1 |