Variant #0000516402 (NC_000002.11:g.48818912G>C, NM_000233.3:c.*95924C>G (LHCGR))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48818912G>C
DNA change (hg38) g.48591773G>C
Published as STON1-GTF2A1L(NM_172311.2):c.2051G>C (p.R684T)
ISCN -
DB-ID GTF2A1L_000002
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHCGR NM_000233.3 -?/. - c.*95924C>G r.(=) p.(=)
STON1-GTF2A1L NM_001198593.1 -?/. - c.2051G>C r.(?) p.(Arg684Thr)
GTF2A1L NM_006872.3 -?/. - c.-26102G>C r.(?) p.(=)
STON1 NM_006873.3 -?/. - c.2051G>C r.(?) p.(Arg684Thr)


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