Variant #0000530137 (NC_000007.13:g.101870885C>T, NC_000007.13(NM_001913.3):c.1255+32002C>T (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.101870885C>T
DNA change (hg38) g.102227605C>T
Published as CUX1(NM_001202543.1):c.3402C>T (p.S1134=), CUX1(NM_001202543.2):c.3402C>T (p.S1134=)
ISCN -
DB-ID CUX1_000007 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) 0.00067 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 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUX1 NM_001913.3 -?/. - c.1255+32002C>T r.(=) p.(=)


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