Gene >> HSPA8
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227378 |
| Start |
123057892:123057892(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1783C>G |
| AA Mutation |
p.Gln595Glu(p.Q595E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000227378 |
| Start |
123057792:123057792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1883G>A |
| AA Mutation |
p.Gly628Asp(p.G628D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |