Variant #0000962090 (NC_000002.11:g.42990569G>A, NM_012205.2:c.*4008C>T (HAAO))

Chromosome 2
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.42990569G>A
DNA change (hg38) -
Published as OXER1(NM_148962.4):c.751C>T (p.(Arg251Cys))
ISCN -
DB-ID HAAO_000020
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) 0.00045 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HAAO NM_012205.2 -?/. - c.*4008C>T r.(=) p.(=)
MTA3 NM_020744.2 -?/. - c.*54310G>A r.(=) p.(=)
OXER1 NM_148962.4 -?/. - c.751C>T r.(?) p.(Arg251Cys)


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