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CCCGCAGCTCACTTGCCATGGCCTT[C/T]AGCTTGGCCTCGTGGGTCCGCACCT
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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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 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | NP_001257894.1 | |
NM_001270966.1 | 2942 | Silent Mutation | CTA,CTG | L,L 532 | NP_001257895.1 | |
NM_002779.4 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | NP_002770.3 | |
XM_011539968.1 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | XP_011538270.1 | |
XM_011539969.2 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | XP_011538271.1 | |
XM_017016433.1 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | XP_016871922.1 | |
XM_017016434.1 | 2942 | Silent Mutation | CTA,CTG | L,L 911 | XP_016871923.1 |