Variant #0000849882 (NC_000002.11:g.43010449T>G, NC_000002.11(NM_012205.2):c.350+5A>C (HAAO))

Chromosome 2
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.43010449T>G
DNA change (hg38) -
Published as HAAO(NM_012205.3):c.350+5A>C
ISCN -
DB-ID HAAO_000013
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) 0.00067 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HAAO NM_012205.2 -/. - c.350+5A>C r.spl? p.?
MTA3 NM_020744.2 -/. - c.*74190T>G r.(=) p.(=)
OXER1 NM_148962.4 -/. - c.-19130A>C r.(?) p.(=)


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