Gene >> INPP4B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262992 |
| Start |
142145880:142145880(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1680G>T |
| AA Mutation |
p.Lys560Asn(p.K560N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262992 |
| Start |
142237967:142237967(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.733G>A |
| AA Mutation |
p.Asp245Asn(p.D245N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |