Variant #0000529127 (NC_000006.11:g.52878497_52878508del, NM_016513.4:c.1106_1117del (ICK))

Chromosome 6
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.52878497_52878508del
DNA change (hg38) g.53013699_53013710del
Published as ICK(NM_014920.3):c.1106_1117del (p.(Pro369_Leu372del)), ICK(NM_016513.4):c.1106_1117delCAAGCCCGTTGC (p.P369_L372del)
ISCN -
DB-ID ICK_000001 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_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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICK NM_016513.4 -?/. - c.1106_1117del r.(?) p.(Pro369_Leu372del)


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