| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220812 |
| Start |
42374252:42374252(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.523G>C |
| AA Mutation |
p.Val175Leu(p.V175L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220812 |
| Start |
42374769:42374769(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.407G>A |
| AA Mutation |
p.Gly136Asp(p.G136D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000220812 |
| Start |
42374789:42374789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.387A>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |