Variant #0000854496 (NC_000016.9:g.3582814G>A, NM_015041.2:c.1065G>A (CLUAP1))

Chromosome 16
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.3582814G>A
DNA change (hg38) -
Published as CLUAP1(NM_015041.3):c.1065G>A (p.T355=)
ISCN -
DB-ID NLRC3_000007
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) 0.00117 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLUAP1 NM_015041.2 -/. - c.1065G>A r.(?) p.(Thr355=)
NLRC3 NM_178844.2 -/. - c.*9011C>T r.(=) p.(=)


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