Gene >> SPRY2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377102 |
| Start |
80337269:80337269(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.437C>T |
| AA Mutation |
p.Ala146Val(p.A146V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377102 |
| Start |
80337250:80337250(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.456G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |