| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373365 |
| Start |
38702976:38702976(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.79A>G |
| AA Mutation |
p.Thr27Ala(p.T27A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373365 |
| Start |
38684432:38684432(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.250G>C |
| AA Mutation |
p.Glu84Gln(p.E84Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373365 |
| Start |
38682863:38682863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.321T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |