| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000268603 |
| Start |
64982161:64982161(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1140C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000268603 |
| Start |
64972059:64972059(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1396C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000268603 |
| Start |
64991782:64991782(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.797delC |
| AA Mutation |
p.Pro266GlnfsTer22(p.P266Qfs*22) |
| Mutation Classification |
Frame_Shift_Del |
| Feature Type |
Transcript |