Variant #0000807056 (NC_000016.9:g.11260273G>A, NM_015226.2:c.2670G>A (CLEC16A))

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.11260273G>A
DNA change (hg38) -
Published as CLEC16A(NM_015226.2):c.2670G>A (p.Q890=), CLEC16A(NM_015226.3):c.2670G>A (p.(Gln890=))
ISCN -
DB-ID CLEC16A_000008 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) 0.00096 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLEC16A NM_015226.2 -?/. - c.2670G>A r.(?) p.(Gln890=)


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