Variant #0000194393 (NC_000002.11:g.233407702C>T, CHRNG(NM_005199.4):c.715C>T)

Individual ID 00117842
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.233407702C>T
DNA change (hg38) g.232542992C>T
Published as -
ISCN -
DB-ID CHRNG_000043 See all 2 reported entries
Variant remarks Homozygote; Previously reported:cDNA 715C->T, Mature protein after signal peptide cleavage R217C.
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Julia Vogt
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNG NM_005199.4 +/+ 7 c.715C>T r.(?) p.(Arg239Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000118305 DNA SEQ - - CHRNG 1 Johan den Dunnen