| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339397 |
| Start |
122020228:122020228(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374380607
|
| CDS Mutation |
c.493A>G |
| AA Mutation |
p.Ile165Val(p.I165V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339397 |
| Start |
122020347:122020347(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.612A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339397 |
| Start |
122022403:122022403(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1101C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |