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- SNP ID:
- rs77389171
- Gene
-
TLR10 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 38774932 - 38774932 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
AAATTGGCTTTTGCCATCTATATTT[G/T]TCATTTCTAATATTTTTGAAGTCTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606270
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Literature Links: |
TLR10 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 |
| TLR10 - toll like receptor 10 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001017388.2 | 791 | Missense Mutation | AAA,ACA | K,T 220 | NP_001017388.1 | |
| NM_001195106.1 | 791 | Missense Mutation | AAA,ACA | K,T 220 | NP_001182035.1 | |
| NM_001195107.1 | 791 | Missense Mutation | AAA,ACA | K,T 220 | NP_001182036.1 | |
| NM_001195108.1 | 791 | Missense Mutation | AAA,ACA | K,T 206 | NP_001182037.1 | |
| NM_030956.3 | 791 | Missense Mutation | AAA,ACA | K,T 220 | NP_112218.2 | |
| XM_011513760.2 | 791 | Missense Mutation | AAA,ACA | K,T 206 | XP_011512062.1 | |
| XM_011513761.2 | 791 | Missense Mutation | AAA,ACA | K,T 220 | XP_011512063.1 | |
| XM_011513762.2 | 791 | Missense Mutation | AAA,ACA | K,T 220 | XP_011512064.1 | |
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