| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000287916 |
| Start |
90413021:90413021(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.345C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000287916 |
| Start |
90412730:90412730(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374340236
|
| CDS Mutation |
c.54C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CLDN12
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287916 |
| Start |
90413278:90413278(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767199576
|
| CDS Mutation |
c.602C>A |
| AA Mutation |
p.Ser201Tyr(p.S201Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|