| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373200 |
| Start |
83509119:83509119(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.795C>A |
| AA Mutation |
p.Ser265Arg(p.S265R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373200 |
| Start |
83508676:83508676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.352C>T |
| AA Mutation |
p.Pro118Ser(p.P118S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373200 |
| Start |
83509101:83509101(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.777G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |