| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376588 |
| Start |
78308421:78308421(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.578T>C |
| AA Mutation |
p.Val193Ala(p.V193A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000376588 |
| Start |
78304760:78304761(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
null
|
| CDS Mutation |
c.222dupT |
| AA Mutation |
p.Leu75SerfsTer26(p.L75Sfs*26) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PSAT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376588 |
| Start |
78302003:78302003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.171G>T |
| AA Mutation |
p.Glu57Asp(p.E57D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|