Gene >> CMTM4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330687 |
| Start |
66636530:66636530(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.238C>T |
| AA Mutation |
p.Pro80Ser(p.P80S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330687 |
| Start |
66622194:66622194(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.491A>T |
| AA Mutation |
p.Tyr164Phe(p.Y164F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |