| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370192 |
| Start |
97740401:97740401(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749699298
|
| CDS Mutation |
c.312T>G |
| AA Mutation |
p.Ile104Met(p.I104M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370192 |
| Start |
97098619:97098619(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2636T>C |
| AA Mutation |
p.Phe879Ser(p.F879S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370192 |
| Start |
97306195:97306195(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145548112
|
| CDS Mutation |
c.2161G>A |
| AA Mutation |
p.Ala721Thr(p.A721T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |