Variant #0000851346 (NC_000007.13:g.101840096A>G, NC_000007.13(NM_001913.3):c.1255+1213A>G (CUX1))

Chromosome 7
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.101840096A>G
DNA change (hg38) -
Published as CUX1(NM_001202543.1):c.1438A>G (p.S480G), CUX1(NM_181552.4):c.1405A>G (p.(Ser469Gly))
ISCN -
DB-ID CUX1_000016 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) 0.00117 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 2022-05-09 15:40:45 +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     
CUX1 NM_001913.3 -?/. - c.1255+1213A>G r.(=) p.(=)


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