| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341776 |
| Start |
15512928:15512928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3149G>A |
| AA Mutation |
p.Arg1050His(p.R1050H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341776 |
| Start |
15512924:15512924(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3145C>T |
| AA Mutation |
p.Arg1049Cys(p.R1049C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341776 |
| Start |
15487420:15487420(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746559577
|
| CDS Mutation |
c.784C>T |
| AA Mutation |
p.Arg262Trp(p.R262W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |