Gene >> HSPA6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000309758 |
| Start |
161524776:161524776(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.118A>G |
| AA Mutation |
p.Thr40Ala(p.T40A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000309758 |
| Start |
161525306:161525306(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.648T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |