| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284885 |
| Start |
18294286:18294286(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2470G>A |
| AA Mutation |
p.Ala824Thr(p.A824T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284885 |
| Start |
18383682:18383682(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.441T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284885 |
| Start |
18294287:18294287(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763270693
|
| CDS Mutation |
c.2469C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |