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TGTTGGAATTTGCTTAAAAATCACA[C/T]GAAAGTGAGAGGCCACGCACAGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604089 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HCST 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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HCST - hematopoietic cell signal transducer | ||||||
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There are no transcripts associated with this gene. |
NFKBID - NFKB inhibitor delta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321831.1 | Intron | NP_001308760.1 | ||||
NM_139239.2 | Intron | NP_640332.1 | ||||
XM_005259340.3 | Intron | XP_005259397.1 | ||||
XM_011527419.2 | Intron | XP_011525721.1 | ||||
XM_011527420.2 | Intron | XP_011525722.1 | ||||
XM_011527421.2 | Intron | XP_011525723.1 | ||||
XM_011527424.2 | Intron | XP_011525726.1 | ||||
XM_017027389.1 | Intron | XP_016882878.1 | ||||
XM_017027390.1 | Intron | XP_016882879.1 | ||||
XM_017027391.1 | Intron | XP_016882880.1 | ||||
XM_017027392.1 | Intron | XP_016882881.1 | ||||
XM_017027393.1 | Intron | XP_016882882.1 | ||||
XM_017027394.1 | Intron | XP_016882883.1 | ||||
XM_017027395.1 | Intron | XP_016882884.1 | ||||
XM_017027396.1 | Intron | XP_016882885.1 | ||||
XM_017027397.1 | Intron | XP_016882886.1 |