| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361611 |
| Start |
23034728:23034728(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.154C>T |
| AA Mutation |
p.Pro52Ser(p.P52S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361611 |
| Start |
23034859:23034859(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.23A>G |
| AA Mutation |
p.Glu8Gly(p.E8G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361611 |
| Start |
23026290:23026290(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.591C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |