Variant #0000990485 (NC_000001.10:g.161202964A>G, NM_001077469.2:c.403T>C (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.161202964A>G
DNA change (hg38) -
Published as NR1I3(NM_001077481.2):c.403T>C (p.(Phe135Leu))
ISCN -
DB-ID NR1I3_000005
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) 1.0E-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 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.403T>C r.(?) p.(Phe135Leu)
NR1I3 NM_005122.4 ?/. - c.403T>C r.(?) p.(Phe135Leu)
TOMM40L NM_032174.4 ?/. - c.*4079A>G r.(=) p.(=)


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