Gene >> TCEAL7
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000332431 |
| Start |
103331471:103331471(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.68G>A |
| AA Mutation |
p.Arg23His(p.R23H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000332431 |
| Start |
103331669:103331669(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.266A>C |
| AA Mutation |
p.Asn89Thr(p.N89T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |