Variant #0000983240 (NC_000019.9:g.14017269_14017277dup, NM_017721.4:c.15_23dup (CC2D1A))

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.14017269_14017277dup
DNA change (hg38) -
Published as CC2D1A(NM_017721.5):c.15_23dup (p.(Pro10_Gly12dup))
ISCN -
DB-ID CC2D1A_000050
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) 0.00047 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D1A NM_017721.4 ?/. - c.15_23dup r.(?) p.(Pro10_Gly12dup)
C19orf57 NM_024323.3 ?/. - c.-427_-419dup r.(?) p.(=)


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