Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCTTACTTACCCCCTCAGGGCCC[A/G]GCCCGGGCCGCAGCAGGTGAACGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NFKBID 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 |
NFKBID - NFKB inhibitor delta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321831.1 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | NP_001308760.1 | |
NM_139239.2 | 1193 | Missense Mutation | CCG,CTG | P,L 292 | NP_640332.1 | |
XM_005259340.3 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | XP_005259397.1 | |
XM_011527419.2 | 1193 | Missense Mutation | CCG,CTG | P,L 444 | XP_011525721.1 | |
XM_011527420.2 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | XP_011525722.1 | |
XM_011527421.2 | 1193 | Missense Mutation | CCG,CTG | P,L 282 | XP_011525723.1 | |
XM_011527424.2 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | XP_011525726.1 | |
XM_017027389.1 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | XP_016882878.1 | |
XM_017027390.1 | 1193 | Missense Mutation | CCG,CTG | P,L 307 | XP_016882879.1 | |
XM_017027391.1 | 1193 | Missense Mutation | CCG,CTG | P,L 292 | XP_016882880.1 | |
XM_017027392.1 | 1193 | Missense Mutation | CCG,CTG | P,L 292 | XP_016882881.1 | |
XM_017027393.1 | 1193 | Missense Mutation | CCG,CTG | P,L 292 | XP_016882882.1 | |
XM_017027394.1 | 1193 | Missense Mutation | CCG,CTG | P,L 282 | XP_016882883.1 | |
XM_017027395.1 | 1193 | Missense Mutation | CCG,CTG | P,L 282 | XP_016882884.1 | |
XM_017027396.1 | 1193 | Intron | XP_016882885.1 | |||
XM_017027397.1 | 1193 | Missense Mutation | CCG,CTG | P,L 259 | XP_016882886.1 |