| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348165 |
| Start |
157181536:157181536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.635A>G |
| AA Mutation |
p.Tyr212Cys(p.Y212C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000348165 |
| Start |
157220709:157220709(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1935A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000348165 |
| Start |
157182276:157182276(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.939T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |