Variant #0000663584 (NC_000003.11:g.93769712C>G, ARL13B(NM_182896.2):c.1186C>G)

Individual ID 00299641
Chromosome 3
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.93769712C>G
DNA change (hg38) g.94050868C>G
Published as -
ISCN -
DB-ID ARL13B_000026 See all 3 reported entries
Variant remarks heterozygous variant only, does not fit phenotype
Reference PubMed: Arno 2017
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0061 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARL13B NM_182896.2 ?/. - c.1186C>G r.(?) p.(Pro396Ala)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000300751 DNA;RNA RT-PCR;SEQ;SEQ-NG - WGS ARHGEF18 48 Johan den Dunnen