Variant #0000689827 (NC_000007.13:g.100160278_100160280dup, NM_006076.4:c.1060_1062dup (AGFG2))

Chromosome 7
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.100160278_100160280dup
DNA change (hg38) -
Published as AGFG2(NM_006076.5):c.1060_1062dupGGC (p.G354dup)
ISCN -
DB-ID AGFG2_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGFG2 NM_006076.4 ?/. - c.1060_1062dup r.(?) p.(Gly354dup)


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