Variant #0000566512 (NC_000019.9:g.17088196C>G, NM_015692.2:c.1881G>C (CPAMD8))

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.17088196C>G
DNA change (hg38) g.16977386C>G
Published as CPAMD8(NM_015692.2):c.1881G>C (p.(Glu627Asp)), CPAMD8(NM_015692.5):c.1740G>C (p.E580D)
ISCN -
DB-ID CPAMD8_000011 See all 2 reported entries
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) 0.00229 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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPAMD8 NM_015692.2 -?/. - c.1881G>C r.(?) p.(Glu627Asp)


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