| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000555044 |
| Start |
73909398:73909398(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.971C>A |
| AA Mutation |
p.Ser324Tyr(p.S324Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000555044 |
| Start |
73904965:73904965(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375182218
|
| CDS Mutation |
c.795G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000555044 |
| Start |
73905058:73905058(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.888G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |