Variant #0000467907 (NC_000001.10:g.147232740C>T, NC_000001.10(NM_005266.6):c.-33-1361G>A (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.147232740C>T
DNA change (hg38) g.147760632=
Published as -
ISCN -
DB-ID GJA5_000012 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs10465885
Origin Germline
Segregation -
Frequency 0.41-0.63
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 13:22:08 +01:00 (CET)
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 ?/. 1i c.-33-1361G>A r.(?) p.(=)


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