Variant #0000566331 (NC_000019.9:g.1465448C>G, NM_005883.2:c.2148C>G (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.1465448C>G
DNA change (hg38) g.1465449C>G
Published as APC2(NM_005883.2):c.2148C>G (p.P716=)
ISCN -
DB-ID APC2_000007
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) 0.00078 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 09:50:53 +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.2148C>G r.(?) p.(Pro716=)
C19orf25 NM_152482.2 -?/. - c.*9583G>C r.(=) p.(=)


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