Colon Cancer: Gene >> RGS13
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000391995 |
| Start |
192659462:192659462(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.419T>A |
| AA Mutation |
p.Phe140Tyr(p.F140Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391995 |
| Start |
192659355:192659355(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149936703
|
| CDS Mutation |
c.312G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RGS13
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000391995 |
| Start |
192659351:192659351(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.308G>T |
| AA Mutation |
p.Ser103Ile(p.S103I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000391995 |
| Start |
192647972:192647972(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.112T>G |
| AA Mutation |
p.Leu38Val(p.L38V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|