Variant #0000786073 (NC_000003.11:g.120393784G>A, NM_000187.3:c.140C>T (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.120393784G>A
DNA change (hg38) g.120674937G>A
Published as S47L
ISCN -
DB-ID HGD_000010
Variant remarks -
Reference Zatkova (2000a) - data and classification copied from HGD mutations database
ClinVar ID -
dbSNP ID rs369517993
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 +/+? 3 c.140C>T r.(?) p.(Ser47Leu)


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