Variant #0000855390 (NC_000019.9:g.1106554C>T, NM_014963.2:c.*1665G>A (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.1106554C>T
DNA change (hg38) -
Published as GPX4(NM_001039847.3):c.599C>T (p.P200L)
ISCN -
DB-ID GPX4_000013
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.688C>T r.(?) p.?
GPX4 NM_002085.3 ?/. - c.577C>T r.(?) p.?
SBNO2 NM_014963.2 ?/. - c.*1665G>A r.(=) p.(=)


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