Variant #0001035082 (NC_000005.9:g.169494563A>G, NM_004946.2:c.4517A>G (DOCK2))

Chromosome 5
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.169494563A>G
DNA change (hg38) -
Published as DOCK2(NM_004946.3):c.4517A>G (p.(Asn1506Ser))
ISCN -
DB-ID DOCK2_000085
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.-88201T>C r.(?) p.(=)
DOCK2 NM_004946.2 ?/. - c.4517A>G r.(?) p.(Asn1506Ser)


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