Variant #0000720367 (NC_000005.9:g.177577962A>G, NM_017838.3:c.263T>C (NHP2))

Chromosome 5
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.177577962A>G
DNA change (hg38) -
Published as NHP2(NM_017838.3):c.263T>C (p.I88T)
ISCN -
DB-ID NHP2_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHP2 NM_017838.3 ?/. - c.263T>C r.(?) p.(Ile88Thr)
RMND5B NM_022762.3 ?/. - c.*2929A>G r.(=) p.(=)


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