Variant #0000338609 (NC_000011.9:g.67226097C>T, NC_000011.9(NM_145200.3):c.800-5C>T (CABP4))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67226097C>T
DNA change (hg38) g.67458626C>T
Published as -
ISCN -
DB-ID CABP4_000012
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) 0.05898 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 09:45:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CABP4 NM_145200.3 -/. - c.800-5C>T r.spl? p.?
GPR152 NM_206997.1 -/. - c.-5902G>A r.(?) p.(=)


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