Variant #0000983792 (NC_000020.10:g.35539668C>G, NM_015474.3:c.1223G>C (SAMHD1))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35539668C>G
DNA change (hg38) -
Published as SAMHD1(NM_015474.4):c.1223G>C (p.(Arg408Pro))
ISCN -
DB-ID C20orf118_000026
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.1223G>C r.(?) p.(Arg408Pro)
C20orf118 NM_080628.1 ?/. - c.*18421C>G r.(=) p.(=)


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