| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345127 |
| Start |
42459993:42459993(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2312A>T |
| AA Mutation |
p.Asp771Val(p.D771V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000345127 |
| Start |
42464473:42464473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1561C>G |
| AA Mutation |
p.Leu521Val(p.L521V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000345127 |
| Start |
42464546:42464546(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1488G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |