| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391807 |
| Start |
50980268:50980268(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147827338
|
| CDS Mutation |
c.441C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391807 |
| Start |
50981889:50981889(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377619320
|
| CDS Mutation |
c.99C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> KLK7
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000391807 |
| Start |
50979835:50979835(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.559T>G |
| AA Mutation |
p.Ser187Ala(p.S187A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391807 |
| Start |
50979863:50979863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142863806
|
| CDS Mutation |
c.531G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|