| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375743 |
| Start |
15943494:15943494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1602G>A |
| AA Mutation |
p.Met534Ile(p.M534I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375743 |
| Start |
15943157:15943157(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1735C>T |
| AA Mutation |
p.His579Tyr(p.H579Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000375743 |
| Start |
15944792:15944792(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.975C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |