| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310581 |
| Start |
1278706:1278706(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs150819225
|
| CDS Mutation |
c.2221G>T |
| AA Mutation |
p.Val741Leu(p.V741L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310581 |
| Start |
1294007:1294007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.879C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310581 |
| Start |
1266514:1266514(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2604T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |