Variant #0000607913 (NC_000002.11:g.32449789T>A, NM_021209.4:c.2828A>T (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.32449789T>A
DNA change (hg38) g.32224720T>A
Published as NLRC4(NM_021209.4):c.2828A>T (p.N943I)
ISCN -
DB-ID NLRC4_000025
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC30A6 NM_001193513.1 ?/. - c.*4007T>A r.(=) p.(=)
NLRC4 NM_021209.4 ?/. - c.2828A>T r.(?) p.(Asn943Ile)


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