| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000276603 |
| Start |
73046082:73046082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1265A>G |
| AA Mutation |
p.Asp422Gly(p.D422G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000276603 |
| Start |
73008924:73008924(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.38G>C |
| AA Mutation |
p.Arg13Pro(p.R13P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000276603 |
| Start |
73032075:73032075(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.981A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |