Colon Cancer: Gene >> PCMT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367384 |
| Start |
149749927:149749927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754551183
|
| CDS Mutation |
c.200G>A |
| AA Mutation |
p.Ser67Asn(p.S67N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367384 |
| Start |
149802239:149802239(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.718C>T |
| AA Mutation |
p.Pro240Ser(p.P240S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PCMT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367384 |
| Start |
149790006:149790006(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.419C>T |
| AA Mutation |
p.Ala140Val(p.A140V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000367384 |
| Start |
149796499:149796499(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769452465
|
| CDS Mutation |
c.677C>T |
| AA Mutation |
p.Ala226Val(p.A226V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|