Variant #0000655349 (NC_000005.9:g.169230163G>A, NM_004946.2:c.2656G>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.169230163G>A
DNA change (hg38) g.169803159G>A
Published as DOCK2(NM_004946.3):c.2656G>A (p.V886I)
ISCN -
DB-ID DOCK2_000036
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) 0.00026 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM196B NM_001129891.1 -?/. - c.*61114C>T r.(=) p.(=)
DOCK2 NM_004946.2 -?/. - c.2656G>A r.(?) p.(Val886Ile)


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