Colon Cancer: Gene >> RSC1A1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345034 |
| Start |
15660007:15660007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776397465
|
| CDS Mutation |
c.139C>T |
| AA Mutation |
p.Arg47Cys(p.R47C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345034 |
| Start |
15660926:15660926(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201454259
|
| CDS Mutation |
c.1058C>T |
| AA Mutation |
p.Thr353Met(p.T353M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RSC1A1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345034 |
| Start |
15661121:15661121(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1253A>C |
| AA Mutation |
p.Gln418Pro(p.Q418P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000345034 |
| Start |
15660789:15660789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.921T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|