Variant #0001050606 (NC_000002.11:g.43010488G>A, NM_012205.2:c.316C>T (HAAO))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.43010488G>A
DNA change (hg38) -
Published as HAAO(NM_012205.3):c.316C>T (p.(Arg106*))
ISCN -
DB-ID HAAO_000026
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.316C>T r.(?) p.(Arg106*)
MTA3 NM_020744.2 ?/. - c.*74229G>A r.(=) p.(=)
OXER1 NM_148962.4 ?/. - c.-19169C>T r.(?) p.(=)


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