Variant #0000002395 (NC_000007.13:g.143048771C>T, CLCN1(NM_000083.2):c.2680C>T)

Individual ID 00002395
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.143048771C>T
Reference Pusch M1, Steinmeyer K, Koch MC, Jentsch TJ.(1995)
DB-ID CLCN1_000013 See all 4 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00297 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
CLCN1 NM_000083.2 ./. 23 c.2680C>T r.(?) p.(Arg894*) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002395 ? ? CLCN1 1 Y Yang