Variant #0001050259 (NC_000001.10:g.151774318A>T, NM_001001523.1:c.*5630T>A (RORC))

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.151774318A>T
DNA change (hg38) -
Published as LINGO4(NM_001004432.4):c.863T>A (p.(Ile288Asn), p.I288N)
ISCN -
DB-ID LINGO4_000003 See all 2 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) 0.00021 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RORC NM_001001523.1 ?/. - c.*5630T>A r.(=) p.(=)
LINGO4 NM_001004432.2 ?/. - c.863T>A r.(?) p.(Ile288Asn)


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