| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368457 |
| Start |
154959309:154959309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.691G>A |
| AA Mutation |
p.Gly231Ser(p.G231S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368457 |
| Start |
154958991:154958991(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1009G>T |
| AA Mutation |
p.Val337Leu(p.V337L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368457 |
| Start |
154959312:154959312(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.688C>T |
| AA Mutation |
p.Pro230Ser(p.P230S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |