Gene >> VIM
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000224237 |
| Start |
17233913:17233913(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.864A>C |
| AA Mutation |
p.Glu288Asp(p.E288D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000224237 |
| Start |
17235329:17235329(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1169A>C |
| AA Mutation |
p.Lys390Thr(p.K390T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |