Gene >> NEU1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375631 |
| Start |
31860216:31860216(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.847A>G |
| AA Mutation |
p.Asn283Asp(p.N283D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000375631 |
| Start |
31862730:31862730(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.47G>T |
| AA Mutation |
p.Gly16Val(p.G16V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |