Variant #0000723052 (NC_000010.10:g.99359925G>T, NC_000010.10(NM_138413.3):c.700+5G>T (HOGA1))

Chromosome 10
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.99359925G>T
DNA change (hg38) -
Published as HOGA1(NM_138413.4):c.700+5G>T
ISCN -
DB-ID C10orf62_000003 See all 3 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) 0.00121 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf62 NM_001009997.2 +/. - c.*9599G>T r.(=) p.(=)
HOGA1 NM_138413.3 +/. - c.700+5G>T r.spl? p.?


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