| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371625 |
| Start |
136979003:136979003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767866230
|
| CDS Mutation |
c.125G>A |
| AA Mutation |
p.Arg42His(p.R42H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371625 |
| Start |
136980046:136980046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.432C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371625 |
| Start |
136977650:136977650(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756456741
|
| CDS Mutation |
c.72G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |