Variant #0000866446 (NC_000020.10:g.35526353del, NM_015474.3:c.1618del (SAMHD1))

Chromosome 20
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.35526353del
DNA change (hg38) -
Published as SAMHD1(NM_001363729.1):c.1513delC (p.L505Ffs*10)
ISCN -
DB-ID C20orf118_000020
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMHD1 NM_015474.3 +/. - c.1618del r.(?) p.(Leu540Phefs*10)
C20orf118 NM_080628.1 +/. - c.*5106del r.(?) p.(=)


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