Variant #0000926994 (NC_000020.10:g.35555634_35555635del, NM_015474.3:c.646_647del (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.35555634_35555635del
DNA change (hg38) -
Published as SAMHD1(NM_015474.3):c.646_647delAT (p.M216Vfs*2), SAMHD1(NM_015474.4):c.646_647delAT (p.M216Vfs*2)
ISCN -
DB-ID C20orf118_000016 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 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 2023-04-16 21:50:28 +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.646_647del r.(?) p.(Met216Valfs*2)
C20orf118 NM_080628.1 +/. - c.*34387_*34388del r.(=) p.(=)


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