CTBS
chitobiase
Summary
Chitobiase is a lysosomal glycosidase involved in degradation of asparagine-linked oligosaccharides on glycoproteins (Aronson and Kuranda, 1989 [PubMed 2531691]).[supplied by OMIM, Nov 2010]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34160527 | 1:85,020,695 | A/G | missense variant | — |
| rs966691223 | 1:85,020,749 | T/C | — | uncertain significance |
| rs138861244 | 1:85,020,769 | G/A | — | benign |
| rs147594119 | 1:85,020,795 | G/A | — | benign |
| rs754461413 | 1:85,029,032 | C/T | — | uncertain significance |
| rs77922958 | 1:85,029,038 | G/A | — | uncertain significance |
| rs138752249 | 1:85,029,068 | G/A | missense variant | — |
| rs1161357596 | 1:85,029,070 | A/G | — | uncertain significance |
| rs143993403 | 1:85,029,085 | A/G | — | likely benign |
| rs987027323 | 1:85,029,098 | G/C | — | uncertain significance |
| rs2527366508 | 1:85,029,437 | G/T | — | uncertain significance |
| rs750617237 | 1:85,029,474 | G/A | — | uncertain significance |
| rs368992334 | 1:85,029,497 | T/C | — | uncertain significance |
| rs757159462 | 1:85,031,526 | G/T | — | uncertain significance |
| rs148319034 | 1:85,035,634 | G/T | — | uncertain significance |
| rs374923690 | 1:85,035,654 | T/C | — | uncertain significance |
| rs759256831 | 1:85,035,714 | A/C | — | uncertain significance |
| rs150587383 | 1:85,035,772 | T/G | — | uncertain significance |
| rs1647255823 | 1:85,035,777 | G/T | — | uncertain significance |
| rs756387712 | 1:85,035,786 | A/G | — | likely benign |
| rs768927936 | 1:85,035,795 | T/C | — | uncertain significance |
| rs1278790935 | 1:85,036,273 | A/G | — | uncertain significance |
| rs754121962 | 1:85,036,321 | T/C | — | uncertain significance |
| rs755196334 | 1:85,036,350 | C/A | — | uncertain significance |
| rs2527383138 | 1:85,036,363 | T/C | — | uncertain significance |
| rs1647276502 | 1:85,036,389 | A/T | — | uncertain significance |
| rs779844966 | 1:85,039,930 | C/G | — | uncertain significance |
| rs545745384 | 1:85,039,997 | C/T | — | benign |
| rs764093334 | 1:85,040,004 | G/A | — | uncertain significance |
| rs749197755 | 1:85,040,037 | C/G | — | uncertain significance |
| rs530177467 | 1:85,040,079 | C/G | — | uncertain significance |
| rs1054563254 | 1:85,040,091 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.