Variant #0000855827 (NC_000020.10:g.35532581C>T, NM_015474.3:c.1482G>A (SAMHD1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35532581C>T
DNA change (hg38) -
Published as SAMHD1(NM_015474.3):c.1482G>A (p.K494=)
ISCN -
DB-ID C20orf118_000021
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) Retrieve
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 15:47:41 +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     
SAMHD1 NM_015474.3 -?/. - c.1482G>A r.(?) p.(Lys494=)
C20orf118 NM_080628.1 -?/. - c.*11334C>T r.(=) p.(=)


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