| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000612778 |
| Start |
155192263:155192263(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.106G>A |
| AA Mutation |
p.Ala36Thr(p.A36T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000612778 |
| Start |
155192111:155192111(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.258T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000612778 |
| Start |
155188376:155188376(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.702delT |
| AA Mutation |
p.Ala235ProfsTer98(p.A235Pfs*98) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |