| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000273261 |
| Start |
66380271:66380271(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3274A>C |
| AA Mutation |
p.Lys1092Gln(p.K1092Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000273261 |
| Start |
66398993:66398993(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1209G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000273261 |
| Start |
66381534:66381534(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2715A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |