Variant #0000925240 (NC_000010.10:g.99358589T>A, NM_138413.3:c.269T>A (HOGA1))

Chromosome 10
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.99358589T>A
DNA change (hg38) -
Published as HOGA1(NM_138413.4):c.269T>A (p.L90H)
ISCN -
DB-ID C10orf62_000005
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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf62 NM_001009997.2 ?/. - c.*8263T>A r.(=) p.(=)
HOGA1 NM_138413.3 ?/. - c.269T>A r.(?) p.(Leu90His)


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