| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310638 |
| Start |
46934460:46934460(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.890T>C |
| AA Mutation |
p.Leu297Ser(p.L297S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310638 |
| Start |
46935586:46935586(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.572T>C |
| AA Mutation |
p.Leu191Ser(p.L191S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310638 |
| Start |
46930169:46930169(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1506C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |