| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000358157 |
| Start |
89001705:89001705(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778344408
|
| CDS Mutation |
c.505G>T |
| AA Mutation |
p.Gly169Cys(p.G169C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358157 |
| Start |
89001218:89001218(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.18G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000358157 |
| Start |
89002196:89002196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138808274
|
| CDS Mutation |
c.996C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |