| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237316 |
| Start |
133889762:133889762(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.365G>A |
| AA Mutation |
p.Arg122Lys(p.R122K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000237316 |
| Start |
133891730:133891730(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.468G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000237316 |
| Start |
133889514:133889514(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.117G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |