Variant #0000981930 (NC_000016.9:g.50763781dup, NM_022162.1:c.3019dup (NOD2))

Chromosome 16
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.50763781dup
DNA change (hg38) -
Published as NOD2(NM_001370466.1):c.2938dup (p.(Leu980ProfsTer2)), NOD2(NM_022162.1):c.3019dupC (p.L1007Pfs*2), NOD2(NM_022162.3):c.3019dupC (p.L1007Pfs*2)
ISCN -
DB-ID NOD2_000043 See all 5 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) Retrieve
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     
NOD2 NM_022162.1 ?/. - c.3019dup r.(?) p.(Leu1007ProfsTer2)


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