| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000305141 |
| Start |
231529008:231529008(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.13T>G |
| AA Mutation |
p.Cys5Gly(p.C5G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305141 |
| Start |
231528169:231528169(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.852G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000305141 |
| Start |
231525352:231525352(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.972A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |