Variant #0000623951 (NC_000019.9:g.17007064C>T, NM_015692.2:c.5490G>A (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.17007064C>T
DNA change (hg38) g.16896253C>T
Published as CPAMD8(NM_015692.4):c.5349G>A (p.Q1783=)
ISCN -
DB-ID F2RL3_000006
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) 0.00226 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-15 15:30:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F2RL3 NM_003950.2 -?/. - c.*5632C>T r.(=) p.(=)
CPAMD8 NM_015692.2 -?/. - c.5490G>A r.(?) p.(Gln1830=)


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