Variant #0000566604 (NC_000019.9:g.1810651C>T, NM_138813.3:c.280G>A (ATP8B3))

Chromosome 19
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.1810651C>T
DNA change (hg38) g.1810652C>T
Published as ATP8B3(NM_001178002.2):c.121G>A (p.(Glu41Lys)), ATP8B3(NM_138813.3):c.280G>A (p.E94K)
ISCN -
DB-ID ATP8B3_000005 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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REXO1 NM_020695.3 -?/. - c.*5414G>A r.(=) p.(=)
ATP8B3 NM_138813.3 -?/. - c.280G>A r.(?) p.(Glu94Lys)


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