| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63323594:63323594(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.536G>A |
| AA Mutation |
p.Arg179Lys(p.R179K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63324366:63324366(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs202214846
|
| CDS Mutation |
c.1308G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371116 |
| Start |
63323493:63323493(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.435G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |