| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000425042 |
| Start |
74961890:74961890(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.711T>G |
| AA Mutation |
p.Phe237Leu(p.F237L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000425042 |
| Start |
74962244:74962244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141799560
|
| CDS Mutation |
c.601G>T |
| AA Mutation |
p.Asp201Tyr(p.D201Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000425042 |
| Start |
74958381:74958381(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143354711
|
| CDS Mutation |
c.1338C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |