Variant #0001015632 (NC_000017.10:g.78075908G>C, NC_000017.10(NM_000152.3):c.-33+219G>C (GAA))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.78075908G>C
DNA change (hg38) -
Published as GAA(NM_000152.3):c.-33+219G>C
ISCN -
DB-ID CCDC40_000211
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 -/. - c.-33+219G>C r.(=) p.(=) -
CCDC40 NM_017950.3 -/. - c.*2334G>C r.(=) p.(=) -


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