Variant #0000275463 (NC_000003.11:g.51251601G>A, NM_004947.4:c.1175G>A (DOCK3))

Chromosome 3
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.51251601G>A
DNA change (hg38) g.51214170G>A
Published as DOCK3(NM_004947.4):c.1175G>A (p.R392Q), DOCK3(NM_004947.5):c.1175G>A (p.R392Q)
ISCN -
DB-ID DOCK3_000005 See all 3 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) 0.00061 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOCK3 NM_004947.4 -?/. - c.1175G>A r.(?) p.(Arg392Gln)


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