| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382361 |
| Start |
5605390:5605390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs568861608
|
| CDS Mutation |
c.1398C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382361 |
| Start |
5593401:5593401(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.465G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382361 |
| Start |
5603915:5603915(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1164C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |