Colon Cancer: Gene >> BLNK
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000224337 |
| Start |
96223900:96223900(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.451T>G |
| AA Mutation |
p.Ser151Ala(p.S151A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000224337 |
| Start |
96242742:96242742(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782546596
|
| CDS Mutation |
c.156C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> BLNK
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000224337 |
| Start |
96192011:96192011(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1333G>T |
| AA Mutation |
p.Asp445Tyr(p.D445Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000224337 |
| Start |
96223901:96223901(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.450C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|