| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303115 |
| Start |
35876471:35876471(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1365C>G |
| AA Mutation |
p.Phe455Leu(p.F455L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303115 |
| Start |
35876423:35876423(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1317T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303115 |
| Start |
35876006:35876006(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.900T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |