Colon Cancer: Gene >> S100B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46602376:46602376(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753432809
|
| CDS Mutation |
c.40G>A |
| AA Mutation |
p.Val14Ile(p.V14I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46602284:46602284(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.132C>A |
| AA Mutation |
p.Phe44Leu(p.F44L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> S100B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46599495:46599495(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.147A>C |
| AA Mutation |
p.Lys49Asn(p.K49N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46599497:46599497(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.145A>G |
| AA Mutation |
p.Lys49Glu(p.K49E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|