| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000622512 |
| Start |
244055034:244055034(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373253112
|
| CDS Mutation |
c.1233G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000622512 |
| Start |
244054357:244054357(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.556C>T |
| AA Mutation |
p.Arg186Ter(p.R186*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ZBTB18
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000622512 |
| Start |
244054499:244054499(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768000553
|
| CDS Mutation |
c.698C>T |
| AA Mutation |
p.Ser233Leu(p.S233L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000622512 |
| Start |
244054357:244054357(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.556C>T |
| AA Mutation |
p.Arg186Ter(p.R186*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|