Gene >> CCR10
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000332438 |
| Start |
42679594:42679594(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1048T>G |
| AA Mutation |
p.Ser350Ala(p.S350A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000332438 |
| Start |
42679851:42679851(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.791G>T |
| AA Mutation |
p.Ser264Ile(p.S264I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |