Product Details
- SNP ID
-
rs147677886
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:46121841 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTAGGTCCATCCAGAACCACCCACT[G/T]CATGCAGAGAAAAACAGTACCTAAT
- Phenotype
-
MIM: 109535
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CD40
PubMed Links
Gene Details
- Gene
- CD40
- Gene Name
- CD40 molecule
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001250.5 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
NP_001241.1 |
NM_001302753.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
NP_001289682.1 |
NM_001322421.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
NP_001309350.1 |
NM_001322422.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
NP_001309351.1 |
NM_152854.3 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
NP_690593.1 |
XM_005260619.3 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
XP_005260676.1 |
XM_011529109.2 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
XP_011527411.1 |
XM_017028135.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
XP_016883624.1 |
XM_017028136.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
XP_016883625.1 |
XM_017028137.1 |
163 |
Missense Mutation |
GCA,TCA |
A25S |
XP_016883626.1 |
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