Variant #0001031410 (NC_000001.10:g.161199675C>T, NC_000001.10(NM_001077469.2):c.933-113G>A (NR1I3))

Chromosome 1
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.161199675C>T
DNA change (hg38) -
Published as NR1I3(NM_005122.5):c.959G>A (p.(Arg320Gln))
ISCN -
DB-ID NR1I3_000007
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) 2.0E-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 2025-05-05 21:14:00 +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.933-113G>A r.(=) p.(=)
NR1I3 NM_005122.4 ?/. - c.959G>A r.(?) p.(Arg320Gln)
TOMM40L NM_032174.4 ?/. - c.*790C>T r.(=) p.(=)


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