Variant #0000272695 (NC_000019.9:g.14017278G>A, NM_017721.4:c.24G>A (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.14017278G>A
DNA change (hg38) g.13906465G>A
Published as CC2D1A(NM_017721.4):c.24G>A (p.P8=)
ISCN -
DB-ID CC2D1A_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 15:16:22 +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.24G>A r.(?) p.(Pro8=)
C19orf57 NM_024323.3 -?/. - c.-428C>T r.(?) p.(=)


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