Variant #0000786106 (NC_000003.11:g.120371492A>G, NM_000187.3:c.289T>C (HGD))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.120371492A>G
DNA change (hg38) g.120652645A>G
Published as W97R
ISCN -
DB-ID HGD_000022
Variant remarks -
Reference Phornphutkul (2002) - data and classification copied from HGD mutations database
ClinVar ID -
dbSNP ID -
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.289T>C r.(?) p.(Trp97Arg)


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