Gene >> FAM84B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304916 |
| Start |
126556927:126556927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.463C>A |
| AA Mutation |
p.Leu155Met(p.L155M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000304916 |
| Start |
126556605:126556605(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.785G>A |
| AA Mutation |
p.Arg262His(p.R262H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |