Gene >> INHBA
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242208 |
| Start |
41690209:41690209(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756546726
|
| CDS Mutation |
c.722G>A |
| AA Mutation |
p.Arg241Gln(p.R241Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000242208 |
| Start |
41690396:41690396(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.535C>T |
| AA Mutation |
p.Gln179Ter(p.Q179*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |