Variant #0000343281 (NC_000010.10:g.99344668C>T, NM_138413.3:c.208C>T (HOGA1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.99344668C>T
DNA change (hg38) g.97584911C>T
Published as -
ISCN -
DB-ID HOGA1_000008
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 09:42:51 +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.-4987C>T r.(?) p.(=)
ANKRD2 NM_001129981.1 +?/. - c.*1186C>T r.(=) p.(=)
HOGA1 NM_138413.3 +?/. - c.208C>T r.(?) p.(Arg70Ter)


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