| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254322 |
| Start |
14516789:14516789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.469C>G |
| AA Mutation |
p.Arg157Gly(p.R157G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254322 |
| Start |
14516067:14516067(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.896G>A |
| AA Mutation |
p.Gly299Glu(p.G299E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254322 |
| Start |
14518192:14518192(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.158A>G |
| AA Mutation |
p.Asp53Gly(p.D53G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |