| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253462 |
| Start |
85678255:85678255(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs192318511
|
| CDS Mutation |
c.515C>T |
| AA Mutation |
p.Thr172Met(p.T172M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253462 |
| Start |
85681636:85681636(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.251T>G |
| AA Mutation |
p.Phe84Cys(p.F84C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GINS2
| Mutation ID |
1 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000253462 |
| Start |
85681614:85681614(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.273C>A |
| AA Mutation |
p.Tyr91Ter(p.Y91*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|