Variant #0000655540 (NC_000006.11:g.169972660_169972665del, NC_000006.11(NM_182552.4):c.2524-9_2524-4del (WDR27))

Chromosome 6
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.169972660_169972665del
DNA change (hg38) g.169572564_169572569del
Published as WDR27(NM_182552.4):c.2524-9_2524-4delTTTTTT
ISCN -
DB-ID WDR27_000003 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-22 13:11:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR27 NM_182552.4 -/. - c.2524-9_2524-4del r.spl? p.?


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