| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000217515 |
| Start |
56618014:56618014(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.482delG |
| AA Mutation |
p.Cys161LeufsTer20(p.C161Lfs*20) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000217515 |
| Start |
56603042:56603042(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
null
|
| CDS Mutation |
c.855delA |
| AA Mutation |
p.Gly286GlufsTer23(p.G286Efs*23) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TXNL1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000217515 |
| Start |
56614459:56614459(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.700C>T |
| AA Mutation |
p.Arg234Cys(p.R234C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000217515 |
| Start |
56624410:56624410(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.247C>T |
| AA Mutation |
p.Arg83Ter(p.R83*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|