Variant #0000300060 (NC_000002.11:g.32449832C>A, NM_021209.4:c.2785G>T (NLRC4))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32449832C>A
DNA change (hg38) g.32224763C>A
Published as NLRC4(NM_021209.4):c.2785G>T (p.A929S)
ISCN -
DB-ID NLRC4_000001 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) 0.00765 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 2018-01-15 20:58:59 +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.*4050C>A r.(=) p.(=)
NLRC4 NM_021209.4 -/. - c.2785G>T r.(?) p.(Ala929Ser)


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