Variant #0000516410 (NC_000002.11:g.48950671C>T, NM_000233.3:c.460G>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.48950671C>T
DNA change (hg38) g.48723532C>T
Published as -
ISCN -
DB-ID GTF2A1L_000009
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHCGR NM_000233.3 ?/. - c.460G>A r.(?) p.(Glu154Lys)
STON1-GTF2A1L NM_001198593.1 ?/. - c.3441+51852C>T r.(=) p.(=)
GTF2A1L NM_006872.3 ?/. - c.*44090C>T r.(=) p.(=)
STON1 NM_006873.3 ?/. - c.*128230C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.