| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216923 |
| Start |
52153201:52153201(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.991C>T |
| AA Mutation |
p.Arg331Trp(p.R331W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216923 |
| Start |
52164753:52164753(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.453C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216923 |
| Start |
52186878:52186878(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.240T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |