Variant #0001051347 (NC_000003.11:g.51418535G>A, NM_004947.4:c.5638G>A (DOCK3))

Chromosome 3
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.51418535G>A
DNA change (hg38) -
Published as DOCK3(NM_004947.5):c.5638G>A (p.(Gly1880Ser))
ISCN -
DB-ID DOCK3_000020
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOCK3 NM_004947.4 ?/. - c.5638G>A r.(?) p.(Gly1880Ser)
MANF NM_006010.4 ?/. - c.-4239G>A r.(?) p.(=)


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