| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367244 |
| Start |
152754244:152754244(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.186A>C |
| AA Mutation |
p.Gln62His(p.Q62H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367244 |
| Start |
152755340:152755340(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.302A>C |
| AA Mutation |
p.Lys101Thr(p.K101T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367244 |
| Start |
152752273:152752273(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.96T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |