| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258243 |
| Start |
229659123:229659123(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4401A>C |
| AA Mutation |
p.Lys1467Asn(p.K1467N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258243 |
| Start |
229635120:229635120(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.507G>T |
| AA Mutation |
p.Leu169Phe(p.L169F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000258243 |
| Start |
229643612:229643612(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3714G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |