| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264156 |
| Start |
135865123:135865123(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.968A>T |
| AA Mutation |
p.Glu323Val(p.E323V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264156 |
| Start |
135851523:135851523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1796A>T |
| AA Mutation |
p.Lys599Ile(p.K599I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264156 |
| Start |
135868810:135868810(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.416G>A |
| AA Mutation |
p.Gly139Glu(p.G139E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |