| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000254868 |
| Start |
7075197:7075197(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200496384
|
| CDS Mutation |
c.808G>A |
| AA Mutation |
p.Asp270Asn(p.D270N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254868 |
| Start |
7075075:7075075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.930G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254868 |
| Start |
7075123:7075123(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139844327
|
| CDS Mutation |
c.882C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |