| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261978 |
| Start |
74529005:74529005(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2105G>T |
| AA Mutation |
p.Gly702Val(p.G702V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261978 |
| Start |
74522809:74522809(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2640C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000261978 |
| Start |
74522007:74522007(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2692G>T |
| AA Mutation |
p.Gly898Ter(p.G898*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |