Colon Cancer: Gene >> HADH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309522 |
| Start |
108033206:108033206(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.740C>T |
| AA Mutation |
p.Ala247Val(p.A247V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309522 |
| Start |
108034275:108034275(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.863A>G |
| AA Mutation |
p.Gln288Arg(p.Q288R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HADH
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309522 |
| Start |
108033181:108033181(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746680125
|
| CDS Mutation |
c.715G>A |
| AA Mutation |
p.Ala239Thr(p.A239T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309522 |
| Start |
108034261:108034261(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.849G>T |
| AA Mutation |
p.Glu283Asp(p.E283D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309522 |
| Start |
108009813:108009813(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.187C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|