| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000321612 |
| Start |
6592200:6592200(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1425A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000321612 |
| Start |
6558589:6558589(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2022G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000321612 |
| Start |
6610207:6610208(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.618_619dupAC |
| AA Mutation |
p.Leu207HisfsTer25(p.L207Hfs*25) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |