| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355237 |
| Start |
69509457:69509457(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.367G>A |
| AA Mutation |
p.Gly123Ser(p.G123S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000355237 |
| Start |
69513971:69513971(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.753C>A |
| AA Mutation |
p.Phe251Leu(p.F251L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000355237 |
| Start |
69509489:69509489(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.399C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |