Variant #0000805849 (NC_000012.11:g.56396395G>A, NM_001032386.1:c.119G>A (SUOX))

Chromosome 12
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.56396395G>A
DNA change (hg38) -
Published as SUOX(NM_000456.2):c.119G>A (p.R40H)
ISCN -
DB-ID IKZF4_000006
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) 0.00035 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
SUOX NM_001032386.1 -?/. 4 c.119G>A r.(?) p.(Arg40His)
IKZF4 NM_022465.3 -?/. - c.-18883G>A r.(?) p.(=)


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