Variant #0000800605 (NC_000002.11:g.42994814C>G, NM_012205.2:c.703G>C (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.42994814C>G
DNA change (hg38) -
Published as HAAO(NM_012205.3):c.703G>C (p.G235R)
ISCN -
DB-ID HAAO_000012
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) 0.00384 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.703G>C r.(?) p.(Gly235Arg)
MTA3 NM_020744.2 ?/. - c.*58555C>G r.(=) p.(=)
OXER1 NM_148962.4 ?/. - c.-3495G>C r.(?) p.(=)


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