Variant #0000467908 (NC_000001.10:g.147246903T>G, NM_005266.6:c.-1581A>C (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.147246903T>G
DNA change (hg38) g.147774791T>G
Published as c.-162-1419A>C
ISCN -
DB-ID GJA5_000014
Variant remarks in perfect LD with -175G>A and -61A>G
Reference -
ClinVar ID -
dbSNP ID rs12408178
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-11-25 14:45:27 +01:00 (CET)
Date last edited 2012-11-25 14:48:04 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJA5 NM_005266.6 ?/. _1 c.-1581A>C r.(=) p.(=)


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