| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117320621:117320621(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.256A>T |
| AA Mutation |
p.Asn86Tyr(p.N86Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117315118:117315118(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.541G>A |
| AA Mutation |
p.Asp181Asn(p.D181N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117320667:117320667(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139486726
|
| CDS Mutation |
c.210C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |