Variant #0000615966 (NC_000016.9:g.3594282C>T, NM_015041.2:c.*8011C>T (CLUAP1))

Chromosome 16
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.3594282C>T
DNA change (hg38) g.3544282C>T
Published as NLRC3(NM_178844.3):c.2819G>A (p.R940H)
ISCN -
DB-ID CLUAP1_000009
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) 0.00019 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLUAP1 NM_015041.2 -?/. - c.*8011C>T r.(=) p.(=)
NLRC3 NM_178844.2 -?/. - c.2819G>A r.(?) p.(Arg940His)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.