Colon Cancer: Gene >> GABARAPL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000037243 |
| Start |
75577313:75577313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.298G>T |
| AA Mutation |
p.Asp100Tyr(p.D100Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000037243 |
| Start |
75568098:75568098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs11556291
|
| CDS Mutation |
c.152T>C |
| AA Mutation |
p.Val51Ala(p.V51A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GABARAPL2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000037243 |
| Start |
75568146:75568146(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.200G>T |
| AA Mutation |
p.Arg67Met(p.R67M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000037243 |
| Start |
75568171:75568171(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.225G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|