| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361923 |
| Start |
7827421:7827421(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2468G>A |
| AA Mutation |
p.Gly823Asp(p.G823D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361923 |
| Start |
7827554:7827554(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2601A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361923 |
| Start |
7827251:7827251(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767649662
|
| CDS Mutation |
c.2298C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |