Colon Cancer: Gene >> SCGB1D4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358585 |
| Start |
62297564:62297564(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.150T>A |
| AA Mutation |
p.Asn50Lys(p.N50K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358585 |
| Start |
62297624:62297624(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.90G>T |
| AA Mutation |
p.Glu30Asp(p.E30D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SCGB1D4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000358585 |
| Start |
62298957:62298957(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.54G>T |
| AA Mutation |
p.Gln18His(p.Q18H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358585 |
| Start |
62297505:62297505(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.209C>A |
| AA Mutation |
p.Ser70Tyr(p.S70Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|