Variant #0000928586 (NC_000002.11:g.32449734A>G, NM_021209.4:c.2883T>C (NLRC4))

Chromosome 2
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.32449734A>G
DNA change (hg38) -
Published as NLRC4(NM_021209.4):c.2883T>C (p.F961=)
ISCN -
DB-ID NLRC4_000052
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) 9.0E-5 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 2023-07-07 10:10:56 +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     
SLC30A6 NM_001193513.1 -?/. - c.*3952A>G r.(=) p.(=)
NLRC4 NM_021209.4 -?/. - c.2883T>C r.(?) p.(Phe961=)


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