Linked Data
ClinVar Variation Id:
2158375
ClinVar RCV Id:
RCV003069737
dbSNP Id:
rs762256695
ExAC:
8:100887781 C / T
gnomAD v2:
8-100887781-C-T
gnomAD v4:
8-99875553-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99875553C>T , CM000670.2:g.99875553C>T | GRCh38 |
| NC_000008.10:g.100887781C>T , CM000670.1:g.100887781C>T | GRCh37 |
| NC_000008.9:g.100956957C>T | NCBI36 |
| NG_007098.2:g.867288C>T , LRG_351:g.867288C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682153.1:c.*1610C>T (VPS13B) | ENSP00000507923.1:n.*1610C>T | |
| ENST00000682358.1:n.12586C>T (VPS13B) | ||
| ENST00000683334.1:c.*7638C>T (VPS13B) | ENSP00000507369.1:n.*7638C>T | |
| ENST00000357162.7:c.11881C>T (VPS13B) MANE Select | ENSP00000349685.2:p.Pro3961Ser | |
| ENST00000358544.7:c.11956C>T (VPS13B) MANE Plus Clinical | ENSP00000351346.2:p.Pro3986Ser | |
| ENST00000357162.6:c.11881C>T (VPS13B) | ENSP00000349685.2:p.Pro3961Ser | |
| ENST00000358544.6:c.11956C>T (VPS13B) | ENSP00000351346.2:p.Pro3986Ser | |
| ENST00000493587.1:n.1458C>T (VPS13B) | ||
| ENST00000520517.5:c.*142-461G>A (COX6C) | ENSP00000429991.1:n.*142-461G>A | |
| ENST00000522934.5:c.*142-2260G>A (COX6C) | ENSP00000428702.1:n.*142-2260G>A | |
| NM_017890.4:c.11956C>T , LRG_351t1:c.11956C>T (VPS13B) | NP_060360.3:p.Pro3986Ser | |
| NM_152564.4:c.11881C>T , LRG_351t2:c.11881C>T (VPS13B) | NP_689777.3:p.Pro3961Ser | |
| XM_005250800.2:c.11956C>T (VPS13B) | XP_005250857.1:p.Pro3986Ser | |
| XM_005250801.3:c.11956C>T (VPS13B) | XP_005250858.1:p.Pro3986Ser | |
| XM_011516848.1:c.11953C>T (VPS13B) | XP_011515150.1:p.Pro3985Ser | |
| XM_011516849.1:c.11878C>T (VPS13B) | XP_011515151.1:p.Pro3960Ser | |
| XM_011516850.1:c.11578C>T (VPS13B) | XP_011515152.1:p.Pro3860Ser | |
| XM_011516851.1:c.8842C>T (VPS13B) | XP_011515153.1:p.Pro2948Ser | |
| XM_011516852.1:c.8842C>T (VPS13B) | XP_011515154.1:p.Pro2948Ser | |
| XM_011516854.1:c.7735C>T (VPS13B) | XP_011515156.1:p.Pro2579Ser | |
| XM_005250800.3:c.11956C>T (VPS13B) | XP_005250857.1:p.Pro3986Ser | |
| XM_005250801.5:c.11956C>T (VPS13B) | XP_005250858.1:p.Pro3986Ser | |
| XM_011516848.2:c.11953C>T (VPS13B) | XP_011515150.1:p.Pro3985Ser | |
| XM_011516849.2:c.11878C>T (VPS13B) | XP_011515151.1:p.Pro3960Ser | |
| XM_011516850.2:c.11578C>T (VPS13B) | XP_011515152.1:p.Pro3860Ser | |
| XM_011516851.2:c.8842C>T (VPS13B) | XP_011515153.1:p.Pro2948Ser | |
| XM_011516852.2:c.8842C>T (VPS13B) | XP_011515154.1:p.Pro2948Ser | |
| XM_011516854.2:c.7735C>T (VPS13B) | XP_011515156.1:p.Pro2579Ser | |
| XM_017013109.1:c.11761C>T (VPS13B) | XP_016868598.1:p.Pro3921Ser | |
| XM_017013111.1:c.8842C>T (VPS13B) | XP_016868600.1:p.Pro2948Ser | |
| XM_017013112.1:c.7513C>T (VPS13B) | XP_016868601.1:p.Pro2505Ser | |
| XM_024447074.1:c.10741C>T (VPS13B) | XP_024302842.1:p.Pro3581Ser | |
| NM_017890.5:c.11956C>T (VPS13B) MANE Plus Clinical | NP_060360.3:p.Pro3986Ser | |
| NM_152564.5:c.11881C>T (VPS13B) MANE Select | NP_689777.3:p.Pro3961Ser |