Variant #0000326043 (NC_000019.9:g.1482902G>T, NM_005883.2:c.*12690G>T (APC2))

Chromosome 19
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.1482902G>T
DNA change (hg38) g.1482903G>T
Published as PCSK4(NM_017573.3):c.1689C>A (p.(Phe563Leu))
ISCN -
DB-ID PCSK4_000001
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) 0.00042 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
APC2 NM_005883.2 ?/. - c.*12690G>T r.(=) p.(=)
PCSK4 NM_017573.3 ?/. - c.1689C>A r.(?) p.(Phe563Leu)
C19orf25 NM_152482.2 ?/. - c.-3743C>A r.(?) p.(=)


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