| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262888 |
| Start |
43774238:43774238(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.637C>A |
| AA Mutation |
p.Leu213Ile(p.L213I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262888 |
| Start |
43776602:43776602(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.194T>G |
| AA Mutation |
p.Ile65Ser(p.I65S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262888 |
| Start |
43774203:43774203(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.672C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |