| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272286 |
| Start |
43875180:43875180(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1523T>G |
| AA Mutation |
p.Ile508Ser(p.I508S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000272286 |
| Start |
43846193:43846193(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.204G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000272286 |
| Start |
43872106:43872106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1095G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |