| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372530 |
| Start |
43432686:43432686(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.706G>T |
| AA Mutation |
p.Gly236Trp(p.G236W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372530 |
| Start |
43438705:43438705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2037C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000372530 |
| Start |
43450040:43450040(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4428G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |