Variant #0000681170 (NC_000018.9:g.47788544T>G, NM_145020.3:c.115A>C (CCDC11))

Chromosome 18
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.47788544T>G
DNA change (hg38) -
Published as CFAP53(NM_145020.4):c.115A>C (p.R39=), CFAP53(NM_145020.5):c.115A>C (p.R39=)
ISCN -
DB-ID CCDC11_000015 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) 0.00396 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBD1 NM_015846.3 -?/. - c.*7677A>C r.(=) p.(=)
CCDC11 NM_145020.3 -?/. - c.115A>C r.(?) p.(Arg39=)


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