| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261908 |
| Start |
73249695:73249695(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1868A>G |
| AA Mutation |
p.Asp623Gly(p.D623G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261908 |
| Start |
73236429:73236429(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763026515
|
| CDS Mutation |
c.1374G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000261908 |
| Start |
73270180:73270180(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2665C>T |
| AA Mutation |
p.Arg889Ter(p.R889*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |