| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263321 |
| Start |
89295242:89295242(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1466C>T |
| AA Mutation |
p.Thr489Ile(p.T489I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263321 |
| Start |
89177961:89177961(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.8T>A |
| AA Mutation |
p.Leu3Gln(p.L3Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263321 |
| Start |
89191231:89191231(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.849C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |