Gene >> TNF
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000449264 |
| Start |
31577158:31577158(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747115001
|
| CDS Mutation |
c.323G>A |
| AA Mutation |
p.Arg108Gln(p.R108Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000449264 |
| Start |
31577126:31577126(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.291A>T |
| AA Mutation |
p.Gln97His(p.Q97H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |