| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000334134 |
| Start |
69816337:69816337(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.307G>A |
| AA Mutation |
p.Gly103Arg(p.G103R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000334134 |
| Start |
69816333:69816333(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs150581924
|
| CDS Mutation |
c.311G>A |
| AA Mutation |
p.Arg104Gln(p.R104Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000334134 |
| Start |
69810353:69810353(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375708730
|
| CDS Mutation |
c.672C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |