| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000234590 |
| Start |
8868045:8868045(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.253A>G |
| AA Mutation |
p.Thr85Ala(p.T85A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234590 |
| Start |
8868052:8868052(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.246G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000234590 |
| Start |
8867234:8867234(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs569194886
|
| CDS Mutation |
c.327C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |