| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000391945 |
| Start |
45364244:45364244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.806C>T |
| AA Mutation |
p.Thr269Met(p.T269M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391945 |
| Start |
45357671:45357671(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142702501
|
| CDS Mutation |
c.1266C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000391945 |
| Start |
45364446:45364446(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.696C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |