Variant #0000281391 (NC_000010.10:g.99371344C>A, NM_138413.3:c.912C>A (HOGA1))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99371344C>A
DNA change (hg38) g.97611587C>A
Published as HOGA1(NM_138413.4):c.912C>A (p.A304=)
ISCN -
DB-ID HOGA1_000007 See all 2 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) 0.30118 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.*21018C>A r.(=) p.(=)
HOGA1 NM_138413.3 -/. - c.912C>A r.(?) p.(Ala304=)
MORN4 NM_178832.3 -/. - c.*4676G>T r.(=) p.(=)


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