Colon Cancer: Gene >> SOCS2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340600 |
| Start |
93574874:93574874(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.292G>A |
| AA Mutation |
p.Glu98Lys(p.E98K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> SOCS2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340600 |
| Start |
93574869:93574869(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.287G>A |
| AA Mutation |
p.Arg96Gln(p.R96Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340600 |
| Start |
93575161:93575161(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769555868
|
| CDS Mutation |
c.579A>C |
| AA Mutation |
p.Glu193Asp(p.E193D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000340600 |
| Start |
93574927:93574927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.345G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|