Variant #0001020017 (NC_000023.10:g.18690154A>T, NM_000330.3:c.35T>A (RS1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.18690154A>T
DNA change (hg38) g.18672034A>T
Published as Leu12His
ISCN -
DB-ID RS1_000016 See all 15 reported entries
Variant remarks in vitro analysis COS-7 cells shows no RS1 in cellular/secreted fractions, no cleavage signal peptide
Reference PubMed: Vijayasarathy 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
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 2024-12-24 14:36:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RS1 NM_000330.3 +/. - c.35T>A - p.Leu12His


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