VPS37C
VPS37C subunit of ESCRT-I
Summary
VPS37C is a subunit of ESCRT-I (endosomal sorting complex required for transport I), a complex in the class E vacuolar protein sorting (VPS) pathway required for sorting ubiquitinated transmembrane proteins into internal vesicles of multivesicular bodies (Eastman et al., 2005 [PubMed 15509564]).[supplied by OMIM, Mar 2008]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7116493 | 11:60,897,885 | G/A | regulatory region variant | — |
| rs373616362 | 11:60,899,420 | G/T | — | uncertain significance |
| rs1861269799 | 11:60,899,422 | A/G | — | likely benign |
| rs771639980 | 11:60,899,453 | G/C | — | uncertain significance |
| rs199731564 | 11:60,899,531 | T/C | — | uncertain significance |
| rs1024006573 | 11:60,899,584 | G/C | — | uncertain significance |
| rs1861278005 | 11:60,899,662 | T/G | — | uncertain significance |
| rs201435185 | 11:60,899,681 | G/A | — | uncertain significance |
| rs758045042 | 11:60,899,728 | G/A | — | uncertain significance |
| rs776790544 | 11:60,899,779 | G/A | — | uncertain significance |
| rs1861282919 | 11:60,899,785 | T/C | — | uncertain significance |
| rs1398778559 | 11:60,899,825 | C/T | — | uncertain significance |
| rs746287465 | 11:60,899,840 | G/A | — | uncertain significance |
| rs768929755 | 11:60,899,858 | C/T | — | uncertain significance |
| rs755593200 | 11:60,899,912 | C/T | — | uncertain significance |
| rs377533753 | 11:60,899,924 | G/A | — | uncertain significance |
| rs1429797171 | 11:60,899,965 | A/G | — | uncertain significance |
| rs200766323 | 11:60,900,742 | G/C | — | uncertain significance |
| rs746822047 | 11:60,900,760 | C/G | — | uncertain significance |
| rs199807441 | 11:60,901,535 | G/A | — | uncertain significance |
| rs142226902 | 11:60,901,541 | C/T | — | uncertain significance |
| rs201496517 | 11:60,901,658 | G/A | — | uncertain significance |
| rs1426793326 | 11:60,901,679 | C/T | — | uncertain significance |
| rs776745376 | 11:60,906,234 | T/C | — | uncertain significance |
| rs758592858 | 11:60,906,286 | C/A | — | uncertain significance |
| rs508970 | 11:60,906,450 | A/T | — | — |
| rs1320627 | 11:60,907,220 | T/G | — | — |
| rs595158 | 11:60,909,581 | C/A | intron variant | — |
| rs663292 | 11:60,930,038 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.