Gene >> CCL13
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225844 |
| Start |
34358106:34358106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs187454526
|
| CDS Mutation |
c.272G>A |
| AA Mutation |
p.Arg91Gln(p.R91Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000225844 |
| Start |
34358051:34358051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.217A>G |
| AA Mutation |
p.Ile73Val(p.I73V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |