| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369769 |
| Start |
110673585:110673585(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1225G>T |
| AA Mutation |
p.Val409Phe(p.V409F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369769 |
| Start |
110673676:110673676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1134G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369769 |
| Start |
110674003:110674003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.807G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |