Variant #0000269831 (NC_000004.11:g.15482904G>A, NC_000004.11(NM_001080522.2):c.247+453G>A (CC2D2A))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15482904G>A
DNA change (hg38) g.15481280G>A
Published as CC2D2A(NM_001164720.1):c.331G>A (p.(Gly111Arg)), CC2D2A(NM_020785.2):c.*68G>A
ISCN -
DB-ID CC2D2A_000040 See all 2 reported entries
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) 0.02272 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CC2D2A NM_001080522.2 -/. - c.247+453G>A r.(=) p.(=)


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