| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368985 |
| Start |
150747855:150747855(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.818C>T |
| AA Mutation |
p.Thr273Ile(p.T273I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368985 |
| Start |
150750146:150750146(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.653A>C |
| AA Mutation |
p.Lys218Thr(p.K218T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368985 |
| Start |
150751868:150751868(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.540C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |