| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254765 |
| Start |
105161616:105161616(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.294A>C |
| AA Mutation |
p.Gln98His(p.Q98H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254765 |
| Start |
105161838:105161838(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.72G>T |
| AA Mutation |
p.Glu24Asp(p.E24D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254765 |
| Start |
105161658:105161658(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.252G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |