| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000376180 |
| Start |
101692679:101692679(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1110C>A |
| AA Mutation |
p.Asp370Glu(p.D370E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376180 |
| Start |
101583301:101583301(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.813T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000376180 |
| Start |
101714538:101714538(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1380T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |