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- SNP ID:
- rs369147340
- Gene
-
R3HCC1L - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.10: 98234447 - 98234447 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TAAAATTGTTTTTTTGTGTTGCAGA[A/G]AGAAAGGATTTGATATTAAATGGGT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
R3HCC1L 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 |
| R3HCC1L - R3H domain and coiled-coil containing 1 like | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001256619.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | NP_001243548.1 | |
| NM_001256620.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | NP_001243549.1 | |
| NM_001256621.1 | 2355 | Missense Mutation | AAG,GAG | K,E 61 | NP_001243550.1 | |
| NM_014472.4 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | NP_055287.4 | |
| NM_138469.2 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | NP_612478.2 | |
| XM_011539639.1 | 2355 | Missense Mutation | AAG,GAG | K,E 676 | XP_011537941.1 | |
| XM_011539640.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537942.1 | |
| XM_011539641.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537943.1 | |
| XM_011539642.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537944.1 | |
| XM_011539643.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537945.1 | |
| XM_011539644.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537946.1 | |
| XM_011539645.2 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537947.1 | |
| XM_011539646.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537948.1 | |
| XM_011539647.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537949.1 | |
| XM_011539648.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_011537950.1 | |
| XM_011539649.1 | 2355 | Missense Mutation | AAG,GAG | K,E 662 | XP_011537951.1 | |
| XM_017016074.1 | 2355 | Missense Mutation | AAG,GAG | K,E 669 | XP_016871563.1 | |
| XM_017016075.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871564.1 | |
| XM_017016076.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871565.1 | |
| XM_017016077.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871566.1 | |
| XM_017016078.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871567.1 | |
| XM_017016079.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871568.1 | |
| XM_017016080.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871569.1 | |
| XM_017016081.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871570.1 | |
| XM_017016082.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871571.1 | |
| XM_017016083.1 | 2355 | Missense Mutation | AAG,GAG | K,E 655 | XP_016871572.1 | |
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