| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348124 |
| Start |
36498582:36498582(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.355C>A |
| AA Mutation |
p.Pro119Thr(p.P119T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348124 |
| Start |
36494996:36494996(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.658A>G |
| AA Mutation |
p.Thr220Ala(p.T220A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000348124 |
| Start |
36489874:36489874(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1533G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |