Variant #0000808728 (NC_000019.9:g.1483709C>T, NM_005883.2:c.*13497C>T (APC2))

Chromosome 19
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.1483709C>T
DNA change (hg38) -
Published as PCSK4(NM_017573.4):c.1331G>A (p.R444H)
ISCN -
DB-ID APC2_000064
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) 0.00018 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 2021-09-17 14:40:49 +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     
APC2 NM_005883.2 -?/. - c.*13497C>T r.(=) p.(=)
PCSK4 NM_017573.3 -?/. - c.1331G>A r.(?) p.(Arg444His)
C19orf25 NM_152482.2 -?/. - c.-4550G>A r.(?) p.(=)


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