| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358410 |
| Start |
68432283:68432283(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1796G>C |
| AA Mutation |
p.Arg599Pro(p.R599P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358410 |
| Start |
68432498:68432498(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1659C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358410 |
| Start |
68416721:68416721(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3102C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |