| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000367296 |
| Start |
201788636:201788636(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3164A>G |
| AA Mutation |
p.Asp1055Gly(p.D1055G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367296 |
| Start |
201788519:201788519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3047C>T |
| AA Mutation |
p.Pro1016Leu(p.P1016L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367296 |
| Start |
201783747:201783747(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2699G>A |
| AA Mutation |
p.Ser900Asn(p.S900N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |