| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000523403 |
| Start |
126646127:126646127(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.398G>C |
| AA Mutation |
p.Cys133Ser(p.C133S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000383572 |
| Start |
126572389:126572389(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.155A>G |
| AA Mutation |
p.Lys52Arg(p.K52R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000523403 |
| Start |
126646117:126646117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.408T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |