Gene >> SNX6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362031 |
| Start |
34603398:34603398(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs530960694
|
| CDS Mutation |
c.502A>G |
| AA Mutation |
p.Ile168Val(p.I168V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362031 |
| Start |
34567690:34567690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1199C>T |
| AA Mutation |
p.Ala400Val(p.A400V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |