| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301178 |
| Start |
41259617:41259617(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2398C>T |
| AA Mutation |
p.Arg800Trp(p.R800W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301178 |
| Start |
41221215:41221215(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs540192002
|
| CDS Mutation |
c.378C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301178 |
| Start |
41248804:41248804(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1695T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |