Variant #0000999394 (NC_000011.9:g.67225863C>T, NM_145200.3:c.673C>T (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.67225863C>T
DNA change (hg38) -
Published as CABP4(NM_001300895.1):c.358C>T (p.R120*)
ISCN -
DB-ID CABP4_000028 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CABP4 NM_145200.3 +?/. - c.673C>T r.(?) p.(Arg225Ter)
GPR152 NM_206997.1 +?/. - c.-5668G>A r.(?) p.(=)


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