| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260682 |
| Start |
94942264:94942264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.404G>T |
| AA Mutation |
p.Gly135Val(p.G135V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260682 |
| Start |
94938821:94938821(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.139A>G |
| AA Mutation |
p.Ile47Val(p.I47V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000260682 |
| Start |
94988957:94988957(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1402G>C |
| AA Mutation |
p.Asp468His(p.D468H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |