Variant #0000786108 (NC_000003.11:g.120371490C>T, NM_000187.3:c.291G>A (HGD))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.120371490C>T
DNA change (hg38) g.120652643C>T
Published as W97*
ISCN -
DB-ID HGD_000243
Variant remarks -
Reference clinvar database - data and classification copied from HGD mutations database
ClinVar ID -
dbSNP ID rs766714128
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-05-21 10:09:09 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGD NM_000187.3 +/+ 5 c.291G>A r.(?) p.(Trp97*)


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