| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73927055:73927055(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.272G>A |
| AA Mutation |
p.Ser91Asn(p.S91N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73942931:73942931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs566197761
|
| CDS Mutation |
c.1180C>T |
| AA Mutation |
p.Arg394Cys(p.R394C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261921 |
| Start |
73942903:73942903(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1152T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |