Variant #0000886737 (NC_000005.9:g.169097598G>A, NM_004946.2:c.221G>A (DOCK2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.169097598G>A
DNA change (hg38) -
Published as DOCK2(NM_004946.3):c.221G>A (p.R74K)
ISCN -
DB-ID DOCK2_000003 See all 2 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) 0.00025 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
FAM196B NM_001129891.1 -?/. - c.*193679C>T r.(=) p.(=)
DOCK2 NM_004946.2 -?/. - c.221G>A r.(?) p.(Arg74Lys)


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