Variant #0000002436 (NC_000007.13:g.143043717delG, CLCN1(NM_000083.2):c.2330delG)

Individual ID 00002436
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.143043717delG
Reference Kuo HC1, Hsiao KM, Chang LI, You TH, Yeh TH, Huang CC.(2006)
DB-ID CLCN1_000056
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 ./. 19 c.2330delG r.(?) p.(Gly777Alafs*17) VariO:0141 DNA deletion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002436 ? ? CLCN1 1 Y Yang