| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26842352:26842352(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1064T>C |
| AA Mutation |
p.Leu355Pro(p.L355P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26839689:26839689(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371016638
|
| CDS Mutation |
c.1926G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284984 |
| Start |
26838088:26838088(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148288841
|
| CDS Mutation |
c.2395T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |