| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254579 |
| Start |
6566689:6566689(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.11309A>G |
| AA Mutation |
p.Tyr3770Cys(p.Y3770C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254579 |
| Start |
6567725:6567725(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375313570
|
| CDS Mutation |
c.12216G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254579 |
| Start |
6570919:6570919(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.13407G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |