| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000398960 |
| Start |
37496210:37496210(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1191G>T |
| AA Mutation |
p.Lys397Asn(p.K397N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000398960 |
| Start |
37512421:37512421(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2182C>T |
| AA Mutation |
p.Pro728Ser(p.P728S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000398960 |
| Start |
37511940:37511940(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1701T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |