| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27648916:27648916(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1002G>T |
| AA Mutation |
p.Arg334Ser(p.R334S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27640752:27640752(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.312G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000395473 |
| Start |
27645890:27645890(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.606C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |