Variant #0000802022 (NC_000005.9:g.169122948G>A, NC_000005.9(NM_004946.2):c.979+6G>A (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.169122948G>A
DNA change (hg38) -
Published as DOCK2(NM_004946.3):c.979+6G>A
ISCN -
DB-ID DOCK2_000054 See all 2 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) 0.00054 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 2021-09-17 14:40:49 +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.*168329C>T r.(=) p.(=)
DOCK2 NM_004946.2 -/. - c.979+6G>A r.(=) p.(=)


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