Variant #0000939931 (NC_000016.9:g.1502857C>T, NM_001287.5:c.1252G>A (CLCN7))

Chromosome 16
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.1502857C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CLCN7_000002 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs12926089
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.07647 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-03 12:21:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN7 NM_001287.5 -/. - c.1252G>A r.(?) p.(Val418Met)


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