Gene >> SPRED2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356388 |
| Start |
65313772:65313772(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.986C>T |
| AA Mutation |
p.Ala329Val(p.A329V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356388 |
| Start |
65313549:65313549(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369939169
|
| CDS Mutation |
c.1209C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |