Gene >> STC2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265087 |
| Start |
173325984:173325984(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770708060
|
| CDS Mutation |
c.178G>A |
| AA Mutation |
p.Ala60Thr(p.A60T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265087 |
| Start |
173317919:173317919(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.837T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |