| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000223028 |
| Start |
123959805:123959805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1366G>A |
| AA Mutation |
p.Asp456Asn(p.D456N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000223028 |
| Start |
123953830:123953830(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.260G>T |
| AA Mutation |
p.Gly87Val(p.G87V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000223028 |
| Start |
123954382:123954382(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.812C>T |
| AA Mutation |
p.Pro271Leu(p.P271L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |