| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255006 |
| Start |
19974899:19974899(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1021A>G |
| AA Mutation |
p.Ser341Gly(p.S341G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000255006 |
| Start |
19990266:19990266(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2170C>A |
| AA Mutation |
p.Leu724Met(p.L724M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000255006 |
| Start |
20000669:20000669(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2568C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |