Variant #0002270531 (NC_000003.11:g.239398G>C, NC_000003.11(NM_006614.3):c.-175+652G>C (CHL1))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.239398G>C
DB-ID -
dbSNP ID rs563726350
gnomAD frequency 21/116238
gnomAD homozygote count 0/58098
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHL1 NM_001253387.1 ./. c.-175+652G>C r.(=) p.(=)
CHL1 NM_006614.3 ./. c.-175+652G>C r.(=) p.(=)