| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306406 |
| Start |
119437012:119437012(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758578873
|
| CDS Mutation |
c.145C>T |
| AA Mutation |
p.His49Tyr(p.H49Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306406 |
| Start |
119437077:119437077(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773227546
|
| CDS Mutation |
c.210G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306406 |
| Start |
119437284:119437284(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148949485
|
| CDS Mutation |
c.417C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |