| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328902 |
| Start |
150628047:150628047(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.551C>A |
| AA Mutation |
p.Ala184Asp(p.A184D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328902 |
| Start |
150628430:150628430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.168A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000328902 |
| Start |
150630109:150630109(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.34G>T |
| AA Mutation |
p.Glu12Ter(p.E12*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |