| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301645 |
| Start |
58491570:58491570(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1420G>C |
| AA Mutation |
p.Ala474Pro(p.A474P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301645 |
| Start |
58491735:58491735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1255A>G |
| AA Mutation |
p.Thr419Ala(p.T419A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301645 |
| Start |
58491682:58491682(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1308C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |