Variant #0000085349 (NC_000001.10:g.228345567C>G, GJC2(NM_020435.3):c.108C>G)

Individual ID 00055375
Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.228345567C>G
DNA change (hg38) g.228157866C>G
Published as 99C>G (I33M)
ISCN -
DB-ID GJC2_000020 See all 2 reported entries
Variant remarks -
Reference PubMed: Orthmann-Murphy 2009, OMIM:var0008
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Michel van Geel
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Michel van Geel
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJC2 NM_020435.3 +/. 2 c.108C>G r.(?) p.(Ile36Met)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000055328 DNA SEQ - - GJC2 2 Michel van Geel