| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000425280 |
| Start |
102111137:102111137(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.181A>T |
| AA Mutation |
p.Thr61Ser(p.T61S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000425280 |
| Start |
102111089:102111089(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.229C>T |
| AA Mutation |
p.Arg77Trp(p.R77W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000425280 |
| Start |
102111102:102111102(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.216T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |