Variant #0000890115 (NC_000011.9:g.67222963G>A, NM_145200.3:c.69G>A (CABP4))

Chromosome 11
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.67222963G>A
DNA change (hg38) -
Published as CABP4(NM_145200.5):c.69G>A (p.A23=)
ISCN -
DB-ID CABP4_000044
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) 8.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.69G>A r.(?) p.(Ala23=)
GPR152 NM_206997.1 -?/. - c.-2768C>T r.(?) p.(=)


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