Variant #0001001896 (NC_000016.9:g.1497386_1497393dup, NC_000016.9(NM_001287.5):c.2250_2250+7dup (CLCN7))

Chromosome 16
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.1497386_1497393dup
DNA change (hg38) -
Published as CLCN7(NM_001287.5):c.2250_2250+7dupGGCATGTG (p.?)
ISCN -
DB-ID CCDC154_000031
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
CCDC154 NM_001143980.1 -?/. - c.-3070_-3063dup r.(?) p.(=)
CLCN7 NM_001287.5 -?/. - c.2250_2250+7dup r.spl? p.?


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