| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361361 |
| Start |
155250692:155250692(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1094G>A |
| AA Mutation |
p.Arg365His(p.R365H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361361 |
| Start |
155254786:155254786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.92T>G |
| AA Mutation |
p.Leu31Arg(p.L31R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000361361 |
| Start |
155250799:155250799(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.987G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |