Colon Cancer: Gene >> PDGFB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000331163 |
| Start |
39243927:39243927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.37T>C |
| AA Mutation |
p.Cys13Arg(p.C13R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000331163 |
| Start |
39225777:39225777(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.672G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PDGFB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000331163 |
| Start |
39225805:39225805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.644T>C |
| AA Mutation |
p.Val215Ala(p.V215A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000331163 |
| Start |
39231782:39231782(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139127455
|
| CDS Mutation |
c.296C>T |
| AA Mutation |
p.Thr99Met(p.T99M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000331163 |
| Start |
39225751:39225751(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs531185137
|
| CDS Mutation |
c.698C>T |
| AA Mutation |
p.Thr233Met(p.T233M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|