| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000326932 |
| Start |
12008425:12008425(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.158A>G |
| AA Mutation |
p.Glu53Gly(p.E53G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000326932 |
| Start |
11964542:11964542(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.975G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000326932 |
| Start |
11965910:11965910(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.729C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |