Colon Cancer: Gene >> ABHD5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000458276 |
| Start |
43714995:43714995(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.710C>A |
| AA Mutation |
p.Ser237Tyr(p.S237Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000458276 |
| Start |
43714965:43714965(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143489624
|
| CDS Mutation |
c.680G>A |
| AA Mutation |
p.Arg227His(p.R227H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> ABHD5
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000458276 |
| Start |
43702552:43702552(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.471C>A |
| AA Mutation |
p.Phe157Leu(p.F157L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000458276 |
| Start |
43715005:43715005(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.720C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000458276 |
| Start |
43702508:43702508(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.427G>T |
| AA Mutation |
p.Gly143Ter(p.G143*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|