Variant #0000326034 (NC_000019.9:g.1108963C>T, NM_014963.2:c.3431G>A (SBNO2))

Chromosome 19
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.1108963C>T
DNA change (hg38) g.1108964C>T
Published as SBNO2(NM_001100122.1):c.3260G>A (p.(Arg1087Gln))
ISCN -
DB-ID SBNO2_000002
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) 5.0E-5 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 2018-01-15 20:58:59 +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     
GPX4 NM_001039848.1 -?/. - c.*2392C>T r.(=) p.(=)
GPX4 NM_002085.3 -?/. - c.*2392C>T r.(=) p.(=)
SBNO2 NM_014963.2 -?/. - c.3431G>A r.(?) p.(Arg1144Gln)


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