| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371253 |
| Start |
47007276:47007276(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2509T>C |
| AA Mutation |
p.Phe837Leu(p.F837L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371253 |
| Start |
47010164:47010164(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1271T>G |
| AA Mutation |
p.Phe424Cys(p.F424C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371253 |
| Start |
47009164:47009164(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2271G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |