| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336078 |
| Start |
58918360:58918360(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.73G>A |
| AA Mutation |
p.Asp25Asn(p.D25N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336078 |
| Start |
58918557:58918557(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.270T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336078 |
| Start |
58919667:58919667(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1380G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |