Gene >> CPQ
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220763 |
| Start |
96785205:96785205(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.308T>G |
| AA Mutation |
p.Val103Gly(p.V103G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_lost |
| Transcription ID |
ENST00000220763 |
| Start |
97143181:97143181(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1417T>C |
| AA Mutation |
p.Ter473GlnextTer3(p.*473Qext*3) |
| Mutation Classification |
Nonstop_Mutation |
| Feature Type |
Transcript |