| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342014 |
| Start |
15537175:15537175(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1264G>C |
| AA Mutation |
p.Glu422Gln(p.E422Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342014 |
| Start |
15542011:15542011(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1424T>A |
| AA Mutation |
p.Phe475Tyr(p.F475Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000342014 |
| Start |
15541987:15541987(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1400T>C |
| AA Mutation |
p.Leu467Pro(p.L467P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |