Variant #0000617391 (NC_000019.9:g.14037633G>C, NC_000019.9(NM_017721.4):c.2074-1G>C (CC2D1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.14037633G>C
DNA change (hg38) g.13926820G>C
Published as -
ISCN -
DB-ID CC2D1A_000038
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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 15:17:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D1A NM_017721.4 +/. - c.2074-1G>C r.spl? p.?
PODNL1 NM_024825.3 +/. - c.*5885C>G r.(=) p.(=)
DCAF15 NM_138353.2 +/. - c.-25692G>C r.(?) p.(=)


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