Gene >> TRH
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302649 |
| Start |
129977182:129977182(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199889071
|
| CDS Mutation |
c.695G>A |
| AA Mutation |
p.Arg232Gln(p.R232Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302649 |
| Start |
129976903:129976903(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769174350
|
| CDS Mutation |
c.416G>A |
| AA Mutation |
p.Arg139Gln(p.R139Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |