Variant #0000556321 (NC_000015.9:g.96875431_96875437del, NM_021005.3:c.97_103del (NR2F2))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.96875431_96875437del
DNA change (hg38) g.96332202_96332208del
Published as NR2F2(NM_021005.4):c.97_103delCCGCCCG (p.P33Afs*77)
ISCN -
DB-ID NR2F2_000003 See all 3 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-07 10:32:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR2F2 NM_021005.3 +/. - c.97_103del r.(?) p.(Pro33AlafsTer77)


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