Colon Cancer: Gene >> SEPT4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58521325:58521325(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1043G>A |
| AA Mutation |
p.Gly348Asp(p.G348D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58526845:58526845(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.194G>T |
| AA Mutation |
p.Arg65Met(p.R65M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SEPT4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58521287:58521287(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200367887
|
| CDS Mutation |
c.1081C>T |
| AA Mutation |
p.Arg361Trp(p.R361W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58522046:58522046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754556138
|
| CDS Mutation |
c.718G>A |
| AA Mutation |
p.Glu240Lys(p.E240K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58520832:58520832(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147468433
|
| CDS Mutation |
c.1288C>T |
| AA Mutation |
p.Arg430Trp(p.R430W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58522051:58522051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.713G>A |
| AA Mutation |
p.Arg238Gln(p.R238Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317268 |
| Start |
58526760:58526760(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.279C>A |
| AA Mutation |
p.Phe93Leu(p.F93L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|