| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303375 |
| Start |
62679822:62679822(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2218G>A |
| AA Mutation |
p.Glu740Lys(p.E740K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303375 |
| Start |
62677405:62677405(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201376256
|
| CDS Mutation |
c.1971G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000303375 |
| Start |
62689953:62689953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs568390139
|
| CDS Mutation |
c.3633C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |