| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357396 |
| Start |
41797897:41797897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.373A>T |
| AA Mutation |
p.Ile125Leu(p.I125L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357396 |
| Start |
41810860:41810860(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.656C>G |
| AA Mutation |
p.Pro219Arg(p.P219R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000357396 |
| Start |
41796728:41796728(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.51G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |