| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285407 |
| Start |
102651322:102651322(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1010A>G |
| AA Mutation |
p.Asn337Ser(p.N337S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285407 |
| Start |
102652189:102652189(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.245C>G |
| AA Mutation |
p.Pro82Arg(p.P82R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285407 |
| Start |
102651414:102651414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.918G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |