| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379376 |
| Start |
4790539:4790539(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145104204
|
| CDS Mutation |
c.449G>A |
| AA Mutation |
p.Arg150His(p.R150H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379376 |
| Start |
4790533:4790533(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.455G>A |
| AA Mutation |
p.Arg152His(p.R152H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000379376 |
| Start |
4795900:4795900(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777291217
|
| CDS Mutation |
c.202C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |