Colon Cancer: Gene >> MPZL3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278949 |
| Start |
118252290:118252290(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.5A>T |
| AA Mutation |
p.Gln2Leu(p.Q2L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278949 |
| Start |
118240302:118240302(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.149T>C |
| AA Mutation |
p.Leu50Ser(p.L50S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MPZL3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278949 |
| Start |
118235494:118235494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.547A>G |
| AA Mutation |
p.Arg183Gly(p.R183G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000278949 |
| Start |
118237221:118237221(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.280G>A |
| AA Mutation |
p.Gly94Ser(p.G94S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|