| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265960 |
| Start |
125468023:125468023(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766806809
|
| CDS Mutation |
c.1294A>G |
| AA Mutation |
p.Ile432Val(p.I432V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265960 |
| Start |
125543136:125543136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.881T>C |
| AA Mutation |
p.Val294Ala(p.V294A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265960 |
| Start |
125672515:125672515(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.60C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |