Variant #0000272395 (NC_000011.9:g.67223856G>C, NM_145200.3:c.484G>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.67223856G>C
DNA change (hg38) g.67456385G>C
Published as CABP4(NM_145200.3):c.484G>C (p.G162R)
ISCN -
DB-ID CABP4_000006
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.484G>C r.(?) p.(Gly162Arg)
GPR152 NM_206997.1 ?/. - c.-3661C>G r.(?) p.(=)


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