Colon Cancer: Gene >> HIST3H2BB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000620438 |
| Start |
228458158:228458158(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138768347
|
| CDS Mutation |
c.29C>T |
| AA Mutation |
p.Ala10Val(p.A10V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000620438 |
| Start |
228458144:228458144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374757361
|
| CDS Mutation |
c.15C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HIST3H2BB
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000620438 |
| Start |
228458169:228458169(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752662647
|
| CDS Mutation |
c.40G>A |
| AA Mutation |
p.Gly14Ser(p.G14S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000620438 |
| Start |
228458171:228458171(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.42T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|