| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298251 |
| Start |
124921356:124921356(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1033G>A |
| AA Mutation |
p.Ala345Thr(p.A345T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298251 |
| Start |
124924766:124924766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760592475
|
| CDS Mutation |
c.389C>G |
| AA Mutation |
p.Thr130Ser(p.T130S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000298251 |
| Start |
124921378:124921378(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1011G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |