| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000436072 |
| Start |
37916315:37916315(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.223T>C |
| AA Mutation |
p.Phe75Leu(p.F75L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000436072 |
| Start |
37916292:37916292(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750458196
|
| CDS Mutation |
c.246G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000436072 |
| Start |
37914446:37914446(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.453G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |