| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335135 |
| Start |
11757001:11757001(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200167770
|
| CDS Mutation |
c.1064C>G |
| AA Mutation |
p.Thr355Ser(p.T355S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335135 |
| Start |
11758318:11758318(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1172G>A |
| AA Mutation |
p.Gly391Asp(p.G391D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000335135 |
| Start |
11756969:11756969(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755482369
|
| CDS Mutation |
c.1032C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |