Colon Cancer: Gene >> LCN2
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000277480 |
| Start |
128153113:128153113(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774218688
|
| CDS Mutation |
c.591C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000277480 |
| Start |
128150375:128150376(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.275+1_275+2insAAAAAGAAGTGTGACTACTGGATCAGGACT |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LCN2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000277480 |
| Start |
128152204:128152204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368254779
|
| CDS Mutation |
c.497C>T |
| AA Mutation |
p.Ser166Leu(p.S166L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|