Colon Cancer: Gene >> SCGB1D1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306238 |
| Start |
62190322:62190322(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.38C>T |
| AA Mutation |
p.Ala13Val(p.A13V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306238 |
| Start |
62192117:62192117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.117A>C |
| AA Mutation |
p.Lys39Asn(p.K39N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SCGB1D1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306238 |
| Start |
62193413:62193413(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.258G>T |
| AA Mutation |
p.Glu86Asp(p.E86D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|