| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315765 |
| Start |
94106020:94106020(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2935C>G |
| AA Mutation |
p.His979Asp(p.H979D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315765 |
| Start |
94063647:94063647(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.555G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315765 |
| Start |
94070531:94070531(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs557012995
|
| CDS Mutation |
c.1221C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |