Colon Cancer: Gene >> SPANXC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358993 |
| Start |
141242418:141242418(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.40G>A |
| AA Mutation |
p.Val14Ile(p.V14I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> SPANXC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358993 |
| Start |
141241629:141241629(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.182G>T |
| AA Mutation |
p.Arg61Ile(p.R61I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358993 |
| Start |
141241598:141241598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs781789990
|
| CDS Mutation |
c.213C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|