| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225275 |
| Start |
58279917:58279917(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.346G>A |
| AA Mutation |
p.Ala116Thr(p.A116T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225275 |
| Start |
58271764:58271764(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1921G>C |
| AA Mutation |
p.Asp641His(p.D641H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000225275 |
| Start |
58279896:58279896(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.367C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |