| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362010 |
| Start |
157470445:157470445(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.223A>T |
| AA Mutation |
p.Ile75Phe(p.I75F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362010 |
| Start |
157364412:157364412(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1228C>A |
| AA Mutation |
p.Gln410Lys(p.Q410K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362010 |
| Start |
157286642:157286642(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2043A>C |
| AA Mutation |
p.Glu681Asp(p.E681D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |