| Mutation ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000240687 |
| Start |
10801797:10801797(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.774C>A |
| AA Mutation |
p.Tyr258Ter(p.Y258*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
inframe_insertion |
| Transcription ID |
ENST00000240687 |
| Start |
10802299:10802300(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.271_272insAAACCAATCATTTAAGTATCTGGACAC |
| AA Mutation |
p.Thr90_Leu91insGlnThrAsnHisLeuSerIleTrpThr(p.T90_L91insQTNHLSIWT) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TAS2R7
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000240687 |
| Start |
10802121:10802121(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.450G>T |
| AA Mutation |
p.Glu150Asp(p.E150D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|