Gene >> IFNG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229135 |
| Start |
68158016:68158016(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.263G>A |
| AA Mutation |
p.Ser88Asn(p.S88N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229135 |
| Start |
68158043:68158043(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.236T>C |
| AA Mutation |
p.Leu79Pro(p.L79P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |