| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397280 |
| Start |
1980147:1980147(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.451C>G |
| AA Mutation |
p.Leu151Val(p.L151V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000397280 |
| Start |
1979800:1979800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.705A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000397280 |
| Start |
1981150:1981150(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.30G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |