Variant #0000568332 (NC_000019.9:g.54310851T>C, NM_144687.2:c.2141A>G (NLRP12))

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.54310851T>C
DNA change (hg38) g.53807597T>C
Published as NLRP12(NM_001277126.1):c.2144A>G (p.N715S), NLRP12(NM_144687.4):c.2141A>G (p.N714S)
ISCN -
DB-ID NLRP12_000025 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) 0.00342 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP12 NM_144687.2 -?/. - c.2141A>G r.(?) p.(Asn714Ser)


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