Variant #0000261013 (NC_000019.9:g.1468154C>T, NM_005883.2:c.4854C>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.1468154C>T
DNA change (hg38) g.1468155C>T
Published as APC2(NM_005883.2):c.4854C>T (p.S1618=)
ISCN -
DB-ID APC2_000003
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 09:51:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APC2 NM_005883.2 -?/. - c.4854C>T r.(?) p.(Ser1618=)
C19orf25 NM_152482.2 -?/. - c.*6877G>A r.(=) p.(=)


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