Variant #0000855143 (NC_000017.10:g.78073394C>T, NM_000152.3:c.-2328C>T (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.78073394C>T
DNA change (hg38) -
Published as CCDC40(NM_017950.3):c.3249C>T (p.Y1083=)
ISCN -
DB-ID CCDC40_000198
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) 0.00021 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 2022-05-09 15:47:41 +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     

Enzyme activity     
GAA NM_000152.3 -?/. - c.-2328C>T r.(?) p.(=) -
CCDC40 NM_017950.3 -?/. - c.3249C>T r.(?) p.(Tyr1083=) -


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