Variant #0000175053 (NC_000007.13:g.65554101A>G, ASL(NM_000048.3):c.857A>G)

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65554101A>G
DNA change (hg38) g.66089114A>G
Published as -
ISCN -
DB-ID ASL_000027 See all 6 reported entries
Variant remarks -
Reference PubMed: Sampaleanu 2001
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site NciI+
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASL NM_000048.3 +/. 12 c.857A>G r.857a>g p.Gln286Arg