Gene >> CPT2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371486 |
| Start |
53213438:53213438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1820C>T |
| AA Mutation |
p.Ser607Phe(p.S607F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371486 |
| Start |
53210513:53210513(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.839G>A |
| AA Mutation |
p.Ser280Asn(p.S280N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |