| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256999 |
| Start |
49208379:49208379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.31G>C |
| AA Mutation |
p.Ala11Pro(p.A11P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256999 |
| Start |
49192878:49192878(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.428T>C |
| AA Mutation |
p.Leu143Ser(p.L143S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256999 |
| Start |
49208308:49208308(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.102C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |