| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000339948 |
| Start |
182056606:182056606(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1405A>T |
| AA Mutation |
p.Ile469Phe(p.I469F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339948 |
| Start |
182056484:182056484(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1527C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000339948 |
| Start |
182057471:182057471(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.540A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |