Variant #0000848937 (NC_000002.11:g.122288501G>A, NR_023343.1:n.46G>A (RNU4ATAC))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.122288501G>A
DNA change (hg38) -
Published as RNU4ATAC(NR_023343.1):n.46G>A
ISCN -
DB-ID RNU4ATAC_000017 See all 4 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) 0.00013 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLASP1 NM_015282.2 +?/. - c.196-600C>T r.(=) p.(=)
RNU4ATAC NR_023343.1 +?/. - n.46G>A r.(?) -


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