| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338081 |
| Start |
111410878:111410878(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.97C>A |
| AA Mutation |
p.Gln33Lys(p.Q33K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338081 |
| Start |
111410816:111410816(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.159G>T |
| AA Mutation |
p.Glu53Asp(p.E53D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338081 |
| Start |
111401086:111401086(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.852A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |