| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370855 |
| Start |
75339613:75339613(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.70G>T |
| AA Mutation |
p.Asp24Tyr(p.D24Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370855 |
| Start |
75217918:75217918(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1572A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000370855 |
| Start |
75251280:75251280(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.275T>A |
| AA Mutation |
p.Leu92Ter(p.L92*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |