| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369583 |
| Start |
110498339:110498339(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.218C>A |
| AA Mutation |
p.Ala73Glu(p.A73E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369583 |
| Start |
110498262:110498262(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.141C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369583 |
| Start |
110502863:110502863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.522T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |