Variant #0000926128 (NC_000016.9:g.1497039G>A, NM_001287.5:c.2299C>T (CLCN7))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1497039G>A
DNA change (hg38) -
Published as CLCN7(NM_001287.6):c.2299C>T (p.R767W)
ISCN -
DB-ID CCDC154_000026
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +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.-2716C>T r.(?) p.(=)
CLCN7 NM_001287.5 +/. - c.2299C>T r.(?) p.(Arg767Trp)


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