Variant #0000679305 (NC_000011.9:g.67225049G>C, NM_145200.3:c.547G>C (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.67225049G>C
DNA change (hg38) -
Published as CABP4(NM_001300895.1):c.232G>C (p.G78R)
ISCN -
DB-ID CABP4_000027 See all 2 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) 0.00058 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.547G>C r.(?) p.(Gly183Arg)
GPR152 NM_206997.1 ?/. - c.-4854C>G r.(?) p.(=)


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