Variant #0000566334 (NC_000019.9:g.1467667G>C, NM_005883.2:c.4367G>C (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.1467667G>C
DNA change (hg38) g.1467668G>C
Published as APC2(NM_005883.2):c.4367G>C (p.(Arg1456Pro))
ISCN -
DB-ID APC2_000009
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) 0.01225 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 2019-07-18 18:22:55 +02:00 (CEST)
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.4367G>C r.(?) p.(Arg1456Pro)
C19orf25 NM_152482.2 -?/. - c.*7364C>G r.(=) p.(=)


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