| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47084451:47084451(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs782734775
|
| CDS Mutation |
c.197C>T |
| AA Mutation |
p.Ser66Leu(p.S66L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47089786:47089786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.357T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000336169 |
| Start |
47091703:47091703(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.588A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |