ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q22.31(chr15:65258583-65742148)x3
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
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 | |||
CILP | - | - |
GRCh38 GRCh37 |
108 | 123 | |
CLPX | - | - |
GRCh38 GRCh37 |
98 | 113 | |
DPP8 | - | - |
GRCh38 GRCh37 |
35 | 48 | |
IGDCC3 | - | - |
GRCh38 GRCh37 |
52 | 67 | |
IGDCC4 | - | - |
GRCh38 GRCh37 |
89 | 103 | |
KBTBD13 | - | - |
GRCh38 GRCh37 |
588 | 603 | |
MTFMT | - | - |
GRCh38 GRCh37 |
228 | 262 | |
PARP16 | - | - | - |
GRCh38 GRCh37 |
22 | 37 |
PDCD7 | - | - |
GRCh38 GRCh37 |
19 | 48 | |
RASL12 | - | - | - |
GRCh38 GRCh37 |
8 | 92 |
There are 4 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 11, 2018 | RCV000846669.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022