Variant #0001065842 (NC_000012.11:g.120729642_120729643insA, NR_003137.2:n.64_65insT (RNU4-2))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.120729642_120729643insA
DNA change (hg38) -
Published as -
ISCN -
DB-ID RNU4-2_000002 See all 46 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIRT4 NM_012240.2 +/. - c.-10541_-10540insA r.(?) p.(=)
RNU4-2 NR_003137.2 +/. - n.64_65insT r.(?) -


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