Colon Cancer: Gene >> MLANA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381471 |
| Start |
5897631:5897631(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142544535
|
| CDS Mutation |
c.152G>A |
| AA Mutation |
p.Arg51Gln(p.R51Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381471 |
| Start |
5906980:5906980(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.270G>T |
| AA Mutation |
p.Glu90Asp(p.E90D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MLANA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381471 |
| Start |
5897631:5897631(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142544535
|
| CDS Mutation |
c.152G>A |
| AA Mutation |
p.Arg51Gln(p.R51Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000381471 |
| Start |
5897569:5897569(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756181750
|
| CDS Mutation |
c.90C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|