| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000458235 |
| Start |
17836013:17836013(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1825G>T |
| AA Mutation |
p.Asp609Tyr(p.D609Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000458235 |
| Start |
17832664:17832664(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200746503
|
| CDS Mutation |
c.2535C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000458235 |
| Start |
17835138:17835138(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200499852
|
| CDS Mutation |
c.1992G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |