Variant #0000525145 (NC_000005.9:g.169143309_169143310del, NC_000005.9(NM_004946.2):c.2031+3_2031+4del (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.169143309_169143310del
DNA change (hg38) g.169716305_169716306del
Published as DOCK2(NM_004946.3):c.2031+3_2031+4delAA
ISCN -
DB-ID DOCK2_000019
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) 6.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 09:17:08 +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.*147967_*147968del r.(=) p.(=)
DOCK2 NM_004946.2 -?/. - c.2031+3_2031+4del r.spl? p.?


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