| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261796 |
| Start |
149376929:149376929(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.118C>A |
| AA Mutation |
p.Pro40Thr(p.P40T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261796 |
| Start |
149374441:149374441(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777391829
|
| CDS Mutation |
c.471G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261796 |
| Start |
149374447:149374447(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs745448406
|
| CDS Mutation |
c.465G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |