| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382333 |
| Start |
15936542:15936542(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.91C>A |
| AA Mutation |
p.Leu31Ile(p.L31I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382333 |
| Start |
15936493:15936493(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.140A>T |
| AA Mutation |
p.Gln47Leu(p.Q47L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382333 |
| Start |
15936306:15936306(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.327G>T |
| AA Mutation |
p.Glu109Asp(p.E109D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |