Variant #0000613857 (NC_000012.11:g.111785422_111785423insGC, NM_015267.3:c.3754_3755insGC (CUX2))

Chromosome 12
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.111785422_111785423insGC
DNA change (hg38) g.111347618_111347619insGC
Published as CUX2(NM_015267.3):c.3754_3755insGC (p.(Ser1252Cysfs*22))
ISCN -
DB-ID CUX2_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUX2 NM_015267.3 -?/. - c.3754_3755insGC r.(?) p.(Ser1252CysfsTer22)


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