Variant #0000300067 (NC_000019.9:g.56320911C>G, NM_145007.3:c.1065G>C (NLRP11))

Chromosome 19
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.56320911C>G
DNA change (hg38) g.55809545C>G
Published as NLRP11(NM_145007.3):c.1065G>C (p.K355N)
ISCN -
DB-ID NLRP11_000001
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_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     
NLRP4 NM_134444.4 -?/. - c.-27455C>G r.(?) p.(=)
NLRP11 NM_145007.3 -?/. - c.1065G>C r.(?) p.(Lys355Asn)


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