| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337979 |
| Start |
59793462:59793462(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.623T>C |
| AA Mutation |
p.Ile208Thr(p.I208T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337979 |
| Start |
59790559:59790559(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.330G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000337979 |
| Start |
59793418:59793418(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.579G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |