Variant #0000565627 (NC_000019.9:g.1108842G>C, NM_014963.2:c.3552C>G (SBNO2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1108842G>C
DNA change (hg38) g.1108843G>C
Published as SBNO2(NM_001100122.1):c.3381C>G (p.(Asp1127Glu))
ISCN -
DB-ID GPX4_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
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.*2271G>C r.(=) p.(=)
GPX4 NM_002085.3 ?/. - c.*2271G>C r.(=) p.(=)
SBNO2 NM_014963.2 ?/. - c.3552C>G r.(?) p.(Asp1184Glu)


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