Variant #0000654189 (NC_000002.11:g.122288496G>A, NR_023343.1:n.41G>A (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.122288496G>A
DNA change (hg38) g.121530920G>A
Published as RNU4ATAC(NR_023343.1):n.41G>A
ISCN -
DB-ID CLASP1_000011
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) 0.0004 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-09 10:43:08 +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.196-595C>T r.(=) p.(=)
RNU4ATAC NR_023343.1 ?/. - n.41G>A r.(?) -


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