| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262776 |
| Start |
78972591:78972591(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.743C>T |
| AA Mutation |
p.Ala248Val(p.A248V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262776 |
| Start |
78971804:78971804(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752934871
|
| CDS Mutation |
c.1530C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262776 |
| Start |
78973143:78973143(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.456C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |