Gene >> IL11
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264563 |
| Start |
55368887:55368887(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.62C>T |
| AA Mutation |
p.Ala21Val(p.A21V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264563 |
| Start |
55366036:55366036(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.571G>A |
| AA Mutation |
p.Gly191Arg(p.G191R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |