| Mutation ID |
9 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233841610:233841610(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749524750
|
| CDS Mutation |
c.1170C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
10 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000411486 |
| Start |
233840931:233840931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765753648
|
| CDS Mutation |
c.1849C>T |
| AA Mutation |
p.Arg617Ter(p.R617*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HJURP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233840996:233840996(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1784C>A |
| AA Mutation |
p.Ser595Tyr(p.S595Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233841702:233841702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1078C>A |
| AA Mutation |
p.Leu360Ile(p.L360I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233841131:233841131(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1649G>A |
| AA Mutation |
p.Gly550Glu(p.G550E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233841085:233841085(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1695A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000411486 |
| Start |
233841817:233841817(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.963G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|