| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1645826:1645826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.654A>C |
| AA Mutation |
p.Lys218Asn(p.K218N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1645925:1645925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149693351
|
| CDS Mutation |
c.753C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> WNT5B
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1646045:1646045(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754560999
|
| CDS Mutation |
c.873C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|