| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000338745 |
| Start |
18420883:18420883(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.85A>C |
| AA Mutation |
p.Lys29Gln(p.K29Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338745 |
| Start |
18394735:18394735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.933T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000338745 |
| Start |
18415201:18415201(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs61733671
|
| CDS Mutation |
c.549A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |