Variant #0000002393 (NC_000007.13:g.143021563_143021564insG, CLCN1(NM_000083.2):c.831_832insG)

Individual ID 00002393
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.143021563_143021564insG
Reference Nagamitsu S1, Matsuura T, Khajavi M, Armstrong R, Gooch C, Harati Y, Ashizawa T.(2000)
DB-ID CLCN1_000014
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
CLCN1 NM_000083.2 ./. 7 c.831_832insG r.(?) p.(Cys278Valfs*12) VariO:0142 DNA insertion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002393 ? ? CLCN1 1 Y Yang