| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306268 |
| Start |
170106027:170106027(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.70G>C |
| AA Mutation |
p.Glu24Gln(p.E24Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306268 |
| Start |
170106261:170106261(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.304C>T |
| AA Mutation |
p.Leu102Phe(p.L102F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306268 |
| Start |
170106239:170106239(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.282G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |