| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368530 |
| Start |
154191190:154191190(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.239C>T |
| AA Mutation |
p.Ala80Val(p.A80V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368530 |
| Start |
154172922:154172922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.552T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TPM3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368530 |
| Start |
154192001:154192001(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754704140
|
| CDS Mutation |
c.18G>T |
| AA Mutation |
p.Lys6Asn(p.K6N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000368530 |
| Start |
154170699:154170699(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.655G>T |
| AA Mutation |
p.Glu219Ter(p.E219*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|