| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338492 |
| Start |
132198907:132198907(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377151543
|
| CDS Mutation |
c.747G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338492 |
| Start |
132204852:132204852(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368616410
|
| CDS Mutation |
c.1641T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000338492 |
| Start |
132198913:132198913(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.753C>A |
| AA Mutation |
p.Tyr251Ter(p.Y251*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |