| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356545 |
| Start |
37616555:37616555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.215T>A |
| AA Mutation |
p.Val72Glu(p.V72E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356545 |
| Start |
37616515:37616515(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766588002
|
| CDS Mutation |
c.255C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356545 |
| Start |
37616524:37616524(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.246A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |