Variant #0000990486 (NC_000001.10:g.161205733_161205734dup, NM_001077469.2:c.143_144dup (NR1I3))

Chromosome 1
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.161205733_161205734dup
DNA change (hg38) -
Published as NR1I3(NM_001077481.2):c.143_144dupCC (p.(Phe49fs))
ISCN -
DB-ID NR1I3_000006
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 2024-08-28 13:07:21 +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     
NR1I3 NM_001077469.2 -?/. - c.143_144dup r.(?) p.(Phe49Profs*25)
NR1I3 NM_005122.4 -?/. - c.143_144dup r.(?) p.(Phe49Profs*25)
TOMM40L NM_032174.4 -?/. - c.*6848_*6849dup r.(=) p.(=)


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