| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377670 |
| Start |
46321793:46321793(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1162A>G |
| AA Mutation |
p.Ile388Val(p.I388V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377670 |
| Start |
46331180:46331180(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772319491
|
| CDS Mutation |
c.1737C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377670 |
| Start |
46308286:46308286(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373645502
|
| CDS Mutation |
c.429C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |