| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000040877 |
| Start |
234398517:234398517(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4108A>T |
| AA Mutation |
p.Ile1370Phe(p.I1370F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000040877 |
| Start |
234401184:234401184(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.4068A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000040877 |
| Start |
234429532:234429532(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2755C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |