| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121818889:121818889(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1027G>A |
| AA Mutation |
p.Asp343Asn(p.D343N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121818162:121818162(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1132C>G |
| AA Mutation |
p.Arg378Gly(p.R378G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000274026 |
| Start |
121819510:121819510(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.864G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |