| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375654 |
| Start |
31811209:31811209(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.764T>G |
| AA Mutation |
p.Ile255Ser(p.I255S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375654 |
| Start |
31810640:31810640(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1333T>C |
| AA Mutation |
p.Tyr445His(p.Y445H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375654 |
| Start |
31810131:31810131(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1842A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |