Variant #0000607935 (NC_000002.11:g.42997667C>T, NM_012205.2:c.406G>A (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.42997667C>T
DNA change (hg38) g.42770527C>T
Published as HAAO(NM_012205.3):c.406G>A (p.D136N)
ISCN -
DB-ID HAAO_000008
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HAAO NM_012205.2 ?/. - c.406G>A r.(?) p.(Asp136Asn)
MTA3 NM_020744.2 ?/. - c.*61408C>T r.(=) p.(=)
OXER1 NM_148962.4 ?/. - c.-6348G>A r.(?) p.(=)


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