| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249284 |
| Start |
122995237:122995237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs781395838
|
| CDS Mutation |
c.398C>A |
| AA Mutation |
p.Ser133Tyr(p.S133Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249284 |
| Start |
122994944:122994944(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200634681
|
| CDS Mutation |
c.691G>A |
| AA Mutation |
p.Val231Ile(p.V231I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TAS2R16
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249284 |
| Start |
122994803:122994803(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.832C>A |
| AA Mutation |
p.Leu278Met(p.L278M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249284 |
| Start |
122995121:122995121(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765993933
|
| CDS Mutation |
c.514A>C |
| AA Mutation |
p.Asn172His(p.N172H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249284 |
| Start |
122995289:122995289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.346C>A |
| AA Mutation |
p.Leu116Ile(p.L116I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|