Variant #0000507773 (NC_000001.10:g.47748036G>C, NM_001048166.1:c.1229C>G (STIL))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47748036G>C
DNA change (hg38) g.47282364G>C
Published as STIL(NM_001048166.1):c.1229C>G (p.(Pro410Arg)), STIL(NM_001282936.1):c.1229C>G (p.P410R)
ISCN -
DB-ID STIL_000038 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00017 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STIL NM_001048166.1 +?/. - c.1229C>G r.(?) p.(Pro410Arg)


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