Variant #0000886779 (NC_000005.9:g.177578012_177578013del, NC_000005.9(NM_017838.3):c.231-17_231-16del (NHP2))

Chromosome 5
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.177578012_177578013del
DNA change (hg38) -
Published as NHP2(NM_017838.3):c.231-17_231-16delGT
ISCN -
DB-ID NHP2_000023
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
NHP2 NM_017838.3 -?/. - c.231-17_231-16del r.(=) p.(=)
RMND5B NM_022762.3 -?/. - c.*2979_*2980del r.(=) p.(=)


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