Variant #0000617295 (NC_000019.9:g.1105487C>G, NM_014963.2:c.*2732G>C (SBNO2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1105487C>G
DNA change (hg38) g.1105488C>G
Published as GPX4(NM_001039848.1):c.413C>G (p.(Pro138Arg))
ISCN -
DB-ID GPX4_000010
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) 3.0E-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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 09:28:26 +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.413C>G r.(?) p.?
GPX4 NM_002085.3 +?/. - c.302C>G r.(?) p.?
SBNO2 NM_014963.2 +?/. - c.*2732G>C r.(=) p.(=)


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