Variant #0000853119 (NC_000011.9:g.67222941T>C, NM_145200.3:c.47T>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.67222941T>C
DNA change (hg38) -
Published as CABP4(NM_145200.3):c.47T>C (p.I16T)
ISCN -
DB-ID CABP4_000041
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) 5.0E-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 2022-05-09 15:40:45 +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.47T>C r.(?) p.(Ile16Thr)
GPR152 NM_206997.1 ?/. - c.-2746A>G r.(?) p.(=)


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