Variant #0000930986 (NC_000019.9:g.1111619G>A, NC_000019.9(NM_014963.2):c.2701-6C>T (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.1111619G>A
DNA change (hg38) -
Published as SBNO2(NM_001100122.1):c.2530-6C>T (p.(=))
ISCN -
DB-ID GPX4_000016
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 2023-07-07 10:10:56 +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     
GPX4 NM_001039848.1 -?/. - c.*5048G>A r.(=) p.(=)
GPX4 NM_002085.3 -?/. - c.*5048G>A r.(=) p.(=)
SBNO2 NM_014963.2 -?/. - c.2701-6C>T r.(=) p.(=)


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