| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100063555:100063555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1213A>T |
| AA Mutation |
p.Arg405Trp(p.R405W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000360863 |
| Start |
100041914:100041914(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1826C>T |
| AA Mutation |
p.Ser609Leu(p.S609L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360863 |
| Start |
99982069:99982069(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3228T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |