Variant #0000975354 (NC_000002.11:g.48952827C>T, NM_000233.3:c.371G>A (LHCGR))

Chromosome 2
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.48952827C>T
DNA change (hg38) -
Published as LHCGR(NM_000233.3):c.371G>A (p.R124Q), LHCGR(NM_000233.4):c.371G>A (p.(Arg124Gln))
ISCN -
DB-ID GTF2A1L_000010 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) 0.00035 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 2024-04-19 20:27:30 +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     
LHCGR NM_000233.3 ?/. - c.371G>A r.(?) p.(Arg124Gln)
STON1-GTF2A1L NM_001198593.1 ?/. - c.3442-50592C>T r.(=) p.(=)
GTF2A1L NM_006872.3 ?/. - c.*46246C>T r.(=) p.(=)
STON1 NM_006873.3 ?/. - c.*130386C>T r.(=) p.(=)


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