Variant #0000976173 (NC_000004.11:g.15601322A>T, NM_001080522.2:c.4667A>T (CC2D2A))

Chromosome 4
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.15601322A>T
DNA change (hg38) -
Published as CC2D2A(NM_001080522.2):c.4667A>T (p.D1556V), CC2D2A(NM_001378615.1):c.4667A>T (p.(Asp1556Val))
ISCN -
DB-ID CC2D2A_000128 See all 25 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) 0.00021 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     
CC2D2A NM_001080522.2 +/. - c.4667A>T r.(?) p.(Asp1556Val)
FBXL5 NM_001193534.1 +/. - c.*6024T>A r.(=) p.(=)


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