| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000284523 |
| Start |
228059058:228059058(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.652T>A |
| AA Mutation |
p.Trp218Arg(p.W218R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284523 |
| Start |
228050690:228050690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.348C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000284523 |
| Start |
228059156:228059156(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.750C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |