Gene >> TNFRSF25
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356876 |
| Start |
6461657:6461657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1031C>T |
| AA Mutation |
p.Ala344Val(p.A344V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356876 |
| Start |
6461633:6461633(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1055G>A |
| AA Mutation |
p.Arg352His(p.R352H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |