Colon Cancer: Gene >> PLA2G16
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000323646 |
| Start |
63590204:63590204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs202079270
|
| CDS Mutation |
c.283C>T |
| AA Mutation |
p.Arg95Trp(p.R95W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000323646 |
| Start |
63590110:63590110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.377G>A |
| AA Mutation |
p.Arg126His(p.R126H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PLA2G16
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000323646 |
| Start |
63590361:63590361(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs117236760
|
| CDS Mutation |
c.126C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000323646 |
| Start |
63590176:63590176(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.311delT |
| AA Mutation |
p.Val104GlyfsTer5(p.V104Gfs*5) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |
|