| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359396 |
| Start |
142875098:142875098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1189A>G |
| AA Mutation |
p.Ile397Val(p.I397V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000359396 |
| Start |
142876447:142876447(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.723C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000359396 |
| Start |
142876757:142876757(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199768684
|
| CDS Mutation |
c.568C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |