Variant #0000726740 (NC_000017.10:g.78073553C>G, NM_000152.3:c.-2169C>G (GAA))

Chromosome 17
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.78073553C>G
DNA change (hg38) -
Published as CCDC40(NM_017950.3):c.3408C>G (p.L1136=)
ISCN -
DB-ID CCDC40_000187
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) 2.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 -?/. - c.-2169C>G r.(?) p.(=) -
CCDC40 NM_017950.3 -?/. - c.3408C>G r.(?) p.(Leu1136=) -


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