Search
LOADING 
- SNP ID:
- rs772160979
- Gene
-
USH1C - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 17520248 - 17520248 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
ACTGAAAATGGAGGTGAGGATGTGG[G/A]ACGGATGAAGAGAGGAGATGGTAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605242
|
||||||||||||||||||||
Literature Links: |
USH1C PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
| USH1C - USH1 protein network component harmonin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001297764.1 | Intron | NP_001284693.1 | ||||
| NM_005709.3 | Intron | NP_005700.2 | ||||
| NM_153676.3 | Intron | NP_710142.1 | ||||
| XM_011519832.2 | Intron | XP_011518134.1 | ||||
| XM_011519834.2 | Intron | XP_011518136.1 | ||||
| XM_017017072.1 | Intron | XP_016872561.1 | ||||
| XM_017017073.1 | Intron | XP_016872562.1 | ||||
| XM_017017074.1 | Intron | XP_016872563.1 | ||||
| XM_017017075.1 | Intron | XP_016872564.1 | ||||
Back To Top