Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGGGGTCCGCCCCAGCTGCCAACA[A/G]GTGCCGCACGATGGCCTCCTGGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFKBID PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
NFKBID - NFKB inhibitor delta | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321831.1 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | NP_001308760.1 | |
NM_139239.2 | 1117 | Silent Mutation | CTG,TTG | L,L 267 | NP_640332.1 | |
XM_005259340.3 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | XP_005259397.1 | |
XM_011527419.2 | 1117 | Silent Mutation | CTG,TTG | L,L 419 | XP_011525721.1 | |
XM_011527420.2 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | XP_011525722.1 | |
XM_011527421.2 | 1117 | Silent Mutation | CTG,TTG | L,L 257 | XP_011525723.1 | |
XM_011527424.2 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | XP_011525726.1 | |
XM_017027389.1 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | XP_016882878.1 | |
XM_017027390.1 | 1117 | Silent Mutation | CTG,TTG | L,L 282 | XP_016882879.1 | |
XM_017027391.1 | 1117 | Silent Mutation | CTG,TTG | L,L 267 | XP_016882880.1 | |
XM_017027392.1 | 1117 | Silent Mutation | CTG,TTG | L,L 267 | XP_016882881.1 | |
XM_017027393.1 | 1117 | Silent Mutation | CTG,TTG | L,L 267 | XP_016882882.1 | |
XM_017027394.1 | 1117 | Silent Mutation | CTG,TTG | L,L 257 | XP_016882883.1 | |
XM_017027395.1 | 1117 | Silent Mutation | CTG,TTG | L,L 257 | XP_016882884.1 | |
XM_017027396.1 | 1117 | Intron | XP_016882885.1 | |||
XM_017027397.1 | 1117 | Silent Mutation | CTG,TTG | L,L 234 | XP_016882886.1 |