| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000267294 |
| Start |
99965693:99965693(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1676A>T |
| AA Mutation |
p.Asp559Val(p.D559V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000267294 |
| Start |
99970491:99970491(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1185G>T |
| AA Mutation |
p.Glu395Asp(p.E395D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000267294 |
| Start |
99965593:99965593(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1776G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |