ClinVar Genomic variation as it relates to human health
NM_001365951.3(KIF1B):c.3475G>C (p.Gly1159Arg)
Germline
Classification
(3)
Uncertain significance
criteria provided, multiple submitters, no conflicts
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
KIF1B | - | - |
GRCh38 GRCh37 |
2692 | 2969 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 30, 2020 | RCV003485775.2 | |
Uncertain significance (1) |
|
Aug 30, 2022 | RCV003099413.2 | |
Uncertain significance (1) |
|
Aug 2, 2022 | RCV004047763.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 10, 2024