Gene >> ABAT
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268251 |
| Start |
8766265:8766265(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.598A>T |
| AA Mutation |
p.Asn200Tyr(p.N200Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268251 |
| Start |
8772868:8772868(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.905A>G |
| AA Mutation |
p.Asn302Ser(p.N302S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |