Variant #0001042692 (NC_000019.9:g.1467367G>T, NM_005883.2:c.4067G>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.1467367G>T
DNA change (hg38) -
Published as APC2(NM_005883.3):c.4067G>T (p.(Arg1356Leu))
ISCN -
DB-ID APC2_000111
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) 4.0E-5 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 2025-05-05 21:14:00 +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.4067G>T r.(?) p.(Arg1356Leu)
C19orf25 NM_152482.2 ?/. - c.*7664C>A r.(=) p.(=)


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