| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274311 |
| Start |
52801067:52801067(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.673G>A |
| AA Mutation |
p.Ala225Thr(p.A225T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274311 |
| Start |
52801483:52801483(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.801A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274311 |
| Start |
52800718:52800718(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.324C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |