| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000526148 |
| Start |
10799735:10799735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2141G>A |
| AA Mutation |
p.Arg714His(p.R714H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000526148 |
| Start |
10801696:10801696(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1378C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000526148 |
| Start |
10804955:10804955(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.309G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |