| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000388922 |
| Start |
51914016:51914016(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.568C>T |
| AA Mutation |
p.Leu190Phe(p.L190F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000388922 |
| Start |
51915349:51915349(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.897T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000388922 |
| Start |
51913674:51913674(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762047618
|
| CDS Mutation |
c.429C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |