| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000616727 |
| Start |
124913663:124913663(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139580449
|
| CDS Mutation |
c.983A>G |
| AA Mutation |
p.Tyr328Cys(p.Y328C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000616727 |
| Start |
124913676:124913676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.970C>A |
| AA Mutation |
p.Leu324Ile(p.L324I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000616727 |
| Start |
124927863:124927863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.183T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |