| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299440 |
| Start |
36575256:36575256(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1952C>G |
| AA Mutation |
p.Ser651Cys(p.S651C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299440 |
| Start |
36574490:36574490(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs104894289
|
| CDS Mutation |
c.1186C>T |
| AA Mutation |
p.Arg396Cys(p.R396C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000299440 |
| Start |
36575977:36575977(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2673G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |