Variant #0000786064 (NC_000003.11:g.120394521T>C, NC_000003.11(NM_000187.3):c.87+118A>G (HGD))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.120394521T>C
DNA change (hg38) g.120675674T>C
Published as ivs2+118A>G
ISCN -
DB-ID HGD_000127
Variant remarks -
Reference Vilboux (2009) - data and classification copied from HGD mutations database
ClinVar ID -
dbSNP ID rs17140396
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGD NM_000187.3 -?/? 2i c.87+118A>G r.(?) p.(?)


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