| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361600 |
| Start |
102657314:102657314(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3401G>A |
| AA Mutation |
p.Ser1134Asn(p.S1134N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361600 |
| Start |
102655152:102655152(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs144058687
|
| CDS Mutation |
c.1239C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361600 |
| Start |
102657657:102657657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3744C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |