Variant #0000509126 (NC_000002.11:g.122288460A>G, NR_023343.1:n.5A>G (RNU4ATAC))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.122288460A>G
DNA change (hg38) g.121530884A>G
Published as RNU4ATAC(NR_023343.1):n.5A>G
ISCN -
DB-ID CLASP1_000003
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) 0.00023 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-09 10:42:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLASP1 NM_015282.2 ?/. - c.196-559T>C r.(=) p.(=)
RNU4ATAC NR_023343.1 ?/. - n.5A>G r.(?) -


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