Variant #0000541743 (NC_000010.10:g.99342400C>T, NM_138413.3:c.-2061C>T (HOGA1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99342400C>T
DNA change (hg38) g.97582643C>T
Published as ANKRD2(NM_001291218.1):c.1132C>T (p.R378C)
ISCN -
DB-ID ANKRD2_000003
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) 0.00168 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf62 NM_001009997.2 -?/. - c.-7255C>T r.(?) p.(=)
ANKRD2 NM_001129981.1 -?/. - c.775C>T r.(?) p.(Arg259Cys)
HOGA1 NM_138413.3 -?/. - c.-2061C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.