Variant #0000347868 (NC_000002.11:g.48915223C>T, NM_000233.3:c.1713G>A (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.48915223C>T
DNA change (hg38) g.48688084C>T
Published as -
ISCN -
DB-ID LHCGR_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHCGR NM_000233.3 +/. - c.1713G>A r.(?) p.(Met571Ile)
STON1-GTF2A1L NM_001198593.1 +/. - c.3441+16404C>T r.(=) p.(=)
GTF2A1L NM_006872.3 +/. - c.*8642C>T r.(=) p.(=)
STON1 NM_006873.3 +/. - c.*92782C>T r.(=) p.(=)


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