| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229335 |
| Start |
8604307:8604307(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.574G>A |
| AA Mutation |
p.Ala192Thr(p.A192T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229335 |
| Start |
8606991:8606991(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.30G>T |
| AA Mutation |
p.Lys10Asn(p.K10N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000229335 |
| Start |
8605246:8605246(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763771833
|
| CDS Mutation |
c.396C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |