| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358406 |
| Start |
143267639:143267639(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.443C>G |
| AA Mutation |
p.Ser148Cys(p.S148C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358406 |
| Start |
143268817:143268817(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.661G>A |
| AA Mutation |
p.Ala221Thr(p.A221T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358406 |
| Start |
143265080:143265080(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.372C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |