Variant #0000716777 (NC_000001.10:g.147380101_147380112del, GJA8(NM_005267.4):c.19_30del)

Chromosome 1
Allele Unknown
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.147380101_147380112del
DNA change (hg38) -
Published as GJA8(NM_005267.5):c.19_30delCTGGGGAACATC (p.G8_L11del)
ISCN -
DB-ID GJA8_000035
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJA8 NM_005267.4 ?/. - c.19_30del r.(?) p.(Gly8_Leu11del)