| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000615612 |
| Start |
23095766:23095766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.71G>C |
| AA Mutation |
p.Arg24Pro(p.R24P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000615612 |
| Start |
23096377:23096377(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.682C>A |
| AA Mutation |
p.Leu228Ile(p.L228I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000615612 |
| Start |
23096298:23096298(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375941406
|
| CDS Mutation |
c.603C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |