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CTCTGCCCCCAGACAAGGAAGAGGT[G/T]CAGCGGAAGCGGAGGAAGGCCTTGC
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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077494.3 | 1278 | Silent Mutation | GTG,GTT | V,V 335 | NP_001070962.1 | |
NM_001261403.2 | 1278 | Silent Mutation | GTG,GTT | V,V 335 | NP_001248332.1 | |
NM_001288724.1 | 1278 | Silent Mutation | GTG,GTT | V,V 335 | NP_001275653.1 | |
NM_001322934.1 | 1278 | Silent Mutation | GTG,GTT | V,V 335 | NP_001309863.1 | |
NM_001322935.1 | 1278 | Intron | NP_001309864.1 | |||
NM_002502.5 | 1278 | Silent Mutation | GTG,GTT | V,V 335 | NP_002493.3 | |
XM_011539830.2 | 1278 | Silent Mutation | GTG,GTT | V,V 190 | XP_011538132.1 | |
XM_011539831.2 | 1278 | Silent Mutation | GTG,GTT | V,V 190 | XP_011538133.1 | |
XM_017016278.1 | 1278 | Silent Mutation | GTG,GTT | V,V 516 | XP_016871767.1 |
PSD - pleckstrin and Sec7 domain containing | ||||||
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There are no transcripts associated with this gene. |