| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241393 |
| Start |
136114912:136114912(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1016C>A |
| AA Mutation |
p.Ser339Tyr(p.S339Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000241393 |
| Start |
136115374:136115374(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.554T>G |
| AA Mutation |
p.Ile185Ser(p.I185S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000241393 |
| Start |
136115709:136115709(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.219G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |