Variant #0000691152 (NC_000011.9:g.67219806G>T, NM_145200.3:c.-3089G>T (CABP4))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.67219806G>T
DNA change (hg38) -
Published as GPR152(NM_206997.1):c.390C>A (p.C130*)
ISCN -
DB-ID CABP4_000030
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.-3089G>T r.(?) p.(=)
GPR152 NM_206997.1 ?/. - c.390C>A r.(?) p.(Cys130Ter)


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