| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282397 |
| Start |
28327535:28327535(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2723T>G |
| AA Mutation |
p.Ile908Ser(p.I908S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282397 |
| Start |
28389951:28389951(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1814G>A |
| AA Mutation |
p.Ser605Asn(p.S605N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282397 |
| Start |
28334061:28334061(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2557C>A |
| AA Mutation |
p.Pro853Thr(p.P853T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |