| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317799 |
| Start |
26254469:26254469(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.104C>G |
| AA Mutation |
p.Ala35Gly(p.A35G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317799 |
| Start |
26278793:26278793(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.622G>T |
| AA Mutation |
p.Ala208Ser(p.A208S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317799 |
| Start |
26279242:26279242(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.738G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |