Gene >> ABCC11
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356608 |
| Start |
48187286:48187286(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2848G>A |
| AA Mutation |
p.Ala950Thr(p.A950T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356608 |
| Start |
48214888:48214888(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201784880
|
| CDS Mutation |
c.1241C>T |
| AA Mutation |
p.Ala414Val(p.A414V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |