Variant #0000654694 (NC_000002.11:g.48915221G>A, NM_000233.3:c.1715C>T (LHCGR))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48915221G>A
DNA change (hg38) g.48688082G>A
Published as -
ISCN -
DB-ID GTF2A1L_000012
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHCGR NM_000233.3 +/. - c.1715C>T r.(?) p.(Ala572Val)
STON1-GTF2A1L NM_001198593.1 +/. - c.3441+16402G>A r.(=) p.(=)
GTF2A1L NM_006872.3 +/. - c.*8640G>A r.(=) p.(=)
STON1 NM_006873.3 +/. - c.*92780G>A r.(=) p.(=)


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