| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382871 |
| Start |
19993096:19993096(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.24A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382871 |
| Start |
19993132:19993132(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.60G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000382871 |
| Start |
20031432:20031432(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1965G>A |
| AA Mutation |
p.Trp655Ter(p.W655*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |