| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361421 |
| Start |
58939426:58939426(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.287T>A |
| AA Mutation |
p.Leu96Gln(p.L96Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361421 |
| Start |
58838295:58838295(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.710A>G |
| AA Mutation |
p.Lys237Arg(p.K237R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361421 |
| Start |
58939464:58939464(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.249G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |