Colon Cancer: Gene >> HOXB13
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290295 |
| Start |
48728509:48728509(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.85G>A |
| AA Mutation |
p.Ala29Thr(p.A29T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290295 |
| Start |
48726843:48726843(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.802C>T |
| AA Mutation |
p.Arg268Trp(p.R268W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HOXB13
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290295 |
| Start |
48727040:48727040(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.605C>T |
| AA Mutation |
p.Ser202Phe(p.S202F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000290295 |
| Start |
48728560:48728560(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.34G>A |
| AA Mutation |
p.Ala12Thr(p.A12T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000290295 |
| Start |
48727991:48727991(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.601+2T>C |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
|