| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265627 |
| Start |
95394690:95394690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.99A>C |
| AA Mutation |
p.Glu33Asp(p.E33D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265627 |
| Start |
95362450:95362450(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778295748
|
| CDS Mutation |
c.818A>T |
| AA Mutation |
p.Asp273Val(p.D273V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265627 |
| Start |
95362470:95362470(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.798A>C |
| AA Mutation |
p.Leu266Phe(p.L266F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |