| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354570 |
| Start |
136388466:136388466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.453G>T |
| AA Mutation |
p.Gln151His(p.Q151H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354570 |
| Start |
136421771:136421771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.96G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354570 |
| Start |
136383702:136383702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.606A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |