| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000267978 |
| Start |
75364106:75364106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.683C>T |
| AA Mutation |
p.Pro228Leu(p.P228L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000267978 |
| Start |
75359383:75359383(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1991C>T |
| AA Mutation |
p.Pro664Leu(p.P664L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000267978 |
| Start |
75368144:75368144(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.156G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |