| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377038 |
| Start |
10463122:10463122(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.719A>G |
| AA Mutation |
p.His240Arg(p.H240R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377038 |
| Start |
10461518:10461518(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.968C>A |
| AA Mutation |
p.Pro323His(p.P323H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377038 |
| Start |
10467217:10467217(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.414C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |