Variant #0001031233 (NC_000001.10:g.147231061C>A, NM_005266.6:c.286G>T (GJA5))

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.147231061C>A
DNA change (hg38) -
Published as GJA5(NM_005266.6):c.286G>T (p.A96S), GJA5(NM_181703.4):c.286G>T (p.(Ala96Ser))
ISCN -
DB-ID GJA5_000003 See all 6 reported entries
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) 0.00012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJA5 NM_005266.6 ?/. - c.286G>T r.(?) p.(Ala96Ser)


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