| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324447 |
| Start |
135911633:135911633(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2201C>A |
| AA Mutation |
p.Pro734His(p.P734H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324447 |
| Start |
135905264:135905264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.326C>G |
| AA Mutation |
p.Ala109Gly(p.A109G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000324447 |
| Start |
135910162:135910162(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1856G>A |
| AA Mutation |
p.Arg619Lys(p.R619K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |