| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367157 |
| Start |
205303632:205303632(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs561905076
|
| CDS Mutation |
c.1705C>T |
| AA Mutation |
p.Arg569Trp(p.R569W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367157 |
| Start |
205303908:205303908(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762199327
|
| CDS Mutation |
c.1429G>A |
| AA Mutation |
p.Val477Met(p.V477M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367157 |
| Start |
205306227:205306227(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377400744
|
| CDS Mutation |
c.651G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |