Variant #0001042672 (NC_000019.9:g.14038843A>C, NM_017721.4:c.2454A>C (CC2D1A))

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.14038843A>C
DNA change (hg38) -
Published as CC2D1A(NM_017721.5):c.2454A>C (p.(Thr818=))
ISCN -
DB-ID CC2D1A_000061
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 2025-05-05 21:14:00 +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.2454A>C r.(?) p.(=)
PODNL1 NM_024825.3 -?/. - c.*4675T>G r.(=) p.(=)
DCAF15 NM_138353.2 -?/. - c.-24482A>C r.(?) p.(=)


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