Variant #0000886739 (NC_000005.9:g.169141139T>G, NM_004946.2:c.1767T>G (DOCK2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.169141139T>G
DNA change (hg38) -
Published as DOCK2(NM_004946.3):c.1767T>G (p.V589=)
ISCN -
DB-ID DOCK2_000065
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) 0.00235 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.*150138A>C r.(=) p.(=)
DOCK2 NM_004946.2 -/. - c.1767T>G r.(?) p.(Val589=)


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