| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302850 |
| Start |
7117082:7117082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4123A>T |
| AA Mutation |
p.Thr1375Ser(p.T1375S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302850 |
| Start |
7120648:7120648(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3631G>A |
| AA Mutation |
p.Gly1211Arg(p.G1211R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302850 |
| Start |
7122756:7122756(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3387T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |