| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357479 |
| Start |
30947212:30947212(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.594G>T |
| AA Mutation |
p.Gln198His(p.Q198H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357479 |
| Start |
30935269:30935269(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746431353
|
| CDS Mutation |
c.882C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357479 |
| Start |
30905524:30905524(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1923C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |