Variant #0000002385 (NC_000007.13:g.143036620G>T, CLCN1(NM_000083.2):c.1488G>T)

Individual ID 00002385
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.143036620G>T
Reference Lorenz C1, Meyer-Kleine C, Steinmeyer K, Koch MC, Jentsch TJ.(1994)
DB-ID CLCN1_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-5 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 ./. 14 c.1488G>T r.(?) p.(Arg496Ser) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002385 ? ? CLCN1 1 Y Yang