Variant #0000802025 (NC_000005.9:g.169477389G>T, NM_004946.2:c.4201G>T (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.169477389G>T
DNA change (hg38) -
Published as DOCK2(NM_004946.3):c.4201G>T (p.A1401S)
ISCN -
DB-ID DOCK2_000046 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) 0.00037 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 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.-71027C>A r.(?) p.(=)
DOCK2 NM_004946.2 -?/. - c.4201G>T r.(?) p.(Ala1401Ser)


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