VWA5B1 | Mutation | Missense | ENST00000289815.8 |
g.20672051G>A
|
c.2729G>A
|
p.Arg910Gln
|
benign
| HepaRG |
VWA5B1 | Mutation | Missense | ENST00000289815.8 |
g.20640961A>C
|
c.439A>C
|
p.Thr147Pro
|
probably damaging
| SNU475 |
VWA5B1 | Mutation | Missense | ENST00000289815.8 |
g.20659375C>A
|
c.1689C>A
|
p.Phe563Leu
|
probably damaging
| Huh6 |
VWA5B1 | Mutation | Truncating | ENST00000289815.8 |
g.20644099G>T
|
c.640G>T
|
p.Glu214X
|
damaging
| SNU398 |
VWA5B1 | Mutation | Truncating | ENST00000289815.8 |
g.20656879G>A
|
c.1457+4G>A
|
p.?
|
damaging
| SNU761 |