| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311626 |
| Start |
48552392:48552392(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.83G>T |
| AA Mutation |
p.Gly28Val(p.G28V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000311626 |
| Start |
48550682:48550682(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.948C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000311626 |
| Start |
48550940:48550940(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.690G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |