Variant #0000976151 (NC_000004.11:g.15482903C>T, NC_000004.11(NM_001080522.2):c.247+452C>T (CC2D2A))

Chromosome 4
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.15482903C>T
DNA change (hg38) -
Published as CC2D2A(NM_001164720.1):c.330C>T (p.G110=), CC2D2A(NM_001164720.2):c.330C>T (p.G110=), CC2D2A(NM_001164720.3):c.330C>T (p.G110=, p.(Gly110=))
ISCN -
DB-ID CC2D2A_000039 See all 4 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) 0.00202 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.247+452C>T r.(=) p.(=)


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