Colon Cancer: Gene >> PMPCB
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000249269 |
| Start |
103309056:103309056(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148246971
|
| CDS Mutation |
c.954G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> PMPCB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249269 |
| Start |
103312068:103312068(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1342G>C |
| AA Mutation |
p.Glu448Gln(p.E448Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249269 |
| Start |
103300189:103300189(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.339G>C |
| AA Mutation |
p.Lys113Asn(p.K113N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249269 |
| Start |
103298680:103298680(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139269263
|
| CDS Mutation |
c.212C>T |
| AA Mutation |
p.Ser71Leu(p.S71L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|