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Search Thermo Fisher Scientific
CGCTATGGTTCGTCTGCCTCTGCAG[G/T]GCGTCCTCTGGGGCTGCTTGCTGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109535 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD40 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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CD40 - CD40 molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001250.5 | 112 | Missense Mutation | GGC,TGC | G,C 8 | NP_001241.1 | |
NM_001302753.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | NP_001289682.1 | |
NM_001322421.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | NP_001309350.1 | |
NM_001322422.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | NP_001309351.1 | |
NM_152854.3 | 112 | Missense Mutation | GGC,TGC | G,C 8 | NP_690593.1 | |
XM_005260619.3 | 112 | Missense Mutation | GGC,TGC | G,C 8 | XP_005260676.1 | |
XM_011529109.2 | 112 | Missense Mutation | GGC,TGC | G,C 8 | XP_011527411.1 | |
XM_017028135.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | XP_016883624.1 | |
XM_017028136.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | XP_016883625.1 | |
XM_017028137.1 | 112 | Missense Mutation | GGC,TGC | G,C 8 | XP_016883626.1 |