Variant #0000915095 (NC_000019.9:g.1106532C>G, NM_014963.2:c.*1687G>C (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.1106532C>G
DNA change (hg38) -
Published as GPX4(NM_001039847.1):c.584-7C>G (p.(=))
ISCN -
DB-ID GPX4_000014
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) 0.00244 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 2023-01-11 15:44:22 +01:00 (CET)
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.673-7C>G r.(=) p.(=)
GPX4 NM_002085.3 -?/. - c.562-7C>G r.(=) p.(=)
SBNO2 NM_014963.2 -?/. - c.*1687G>C r.(=) p.(=)


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