| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000410096 |
| Start |
157325505:157325505(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.138A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000410096 |
| Start |
157321639:157321639(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.487C>T |
| AA Mutation |
p.Arg163Ter(p.R163*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
inframe_insertion |
| Transcription ID |
ENST00000410096 |
| Start |
157321549:157321550(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
rs778989799
|
| CDS Mutation |
c.574_576dupGAT |
| AA Mutation |
p.Asp192dup(p.D192dup) |
| Mutation Classification |
In_Frame_Ins |
| Feature Type |
Transcript |