Variant #0000545378 (NC_000011.9:g.67226102_67226103del, NM_145200.3:c.800_801del (CABP4))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67226102_67226103del
DNA change (hg38) g.67458631_67458632del
Published as CABP4(NM_001300895.3):c.485-2_485-1delAG
ISCN -
DB-ID CABP4_000014 See all 6 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CABP4 NM_145200.3 +?/. - c.800_801del r.(?) p.(Glu267ValfsTer92)
GPR152 NM_206997.1 +?/. - c.-5906_-5905del r.(?) p.(=)


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