Variant #0000800584 (NC_000002.11:g.32449565C>T, NM_021209.4:c.3052G>A (NLRC4))

Chromosome 2
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.32449565C>T
DNA change (hg38) -
Published as NLRC4(NM_021209.4):c.3052G>A (p.A1018T)
ISCN -
DB-ID NLRC4_000038
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.*3783C>T r.(=) p.(=)
NLRC4 NM_021209.4 ?/. - c.3052G>A r.(?) p.(Ala1018Thr)


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