| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000246069 |
| Start |
17601006:17601006(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.272C>T |
| AA Mutation |
p.Thr91Ile(p.T91I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000246069 |
| Start |
17601034:17601035(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
rs767965259
|
| CDS Mutation |
c.308dupT |
| AA Mutation |
p.Leu103PhefsTer12(p.L103Ffs*12) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> DSTN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000246069 |
| Start |
17600795:17600795(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138670114
|
| CDS Mutation |
c.61C>T |
| AA Mutation |
p.Arg21Cys(p.R21C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|