Colon Cancer: Gene >> LPCAT3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261407 |
| Start |
6981151:6981151(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.530C>T |
| AA Mutation |
p.Ala177Val(p.A177V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261407 |
| Start |
6978479:6978479(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.902G>A |
| AA Mutation |
p.Gly301Asp(p.G301D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LPCAT3
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261407 |
| Start |
6981111:6981111(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.570C>A |
| AA Mutation |
p.Phe190Leu(p.F190L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261407 |
| Start |
6981178:6981178(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.503C>G |
| AA Mutation |
p.Ser168Cys(p.S168C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|