Variant #0000563488 (NC_000017.10:g.78073485G>A, NM_000152.3:c.-2237G>A (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.78073485G>A
DNA change (hg38) g.80099686G>A
Published as CCDC40(NM_017950.3):c.3340G>A (p.V1114M, p.(Val1114Met))
ISCN -
DB-ID CCDC40_000094 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) 0.01477 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 2019-07-18 18:22:55 +02:00 (CEST)
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     

Enzyme activity     
GAA NM_000152.3 ?/. - c.-2237G>A r.(?) p.(=) -
CCDC40 NM_017950.3 ?/. - c.3340G>A r.(?) p.(Val1114Met) -


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