| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000231887 |
| Start |
185229441:185229441(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.454A>G |
| AA Mutation |
p.Ile152Val(p.I152V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000231887 |
| Start |
185193387:185193387(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1011C>A |
| AA Mutation |
p.Asn337Lys(p.N337K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000231887 |
| Start |
185193046:185193046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1352C>T |
| AA Mutation |
p.Ser451Phe(p.S451F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |