Variant #0000983290 (NC_000019.9:g.17007323_17007343dup, NM_015692.2:c.5351_5371dup (CPAMD8))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.17007323_17007343dup
DNA change (hg38) -
Published as CPAMD8(NM_015692.5):c.5210_5230dup (p.(Leu1737_Arg1743dup))
ISCN -
DB-ID F2RL3_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F2RL3 NM_003950.2 ?/. - c.*5891_*5911dup r.(=) p.(=)
CPAMD8 NM_015692.2 ?/. - c.5351_5371dup r.(?) p.(Leu1784_Arg1790dup)


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