| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371144 |
| Start |
124042627:124042627(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.444G>A |
| AA Mutation |
p.Met148Ile(p.M148I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371144 |
| Start |
124047438:124047438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.752A>C |
| AA Mutation |
p.Glu251Ala(p.E251A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371144 |
| Start |
124047454:124047454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.768T>G |
| AA Mutation |
p.Ile256Met(p.I256M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |