Variant #0000285976 (NC_000002.11:g.48925998del, NC_000002.11(NM_000233.3):c.681-48del (LHCGR))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48925998del
DNA change (hg38) g.48698859del
Published as LHCGR(NM_000233.4):c.681-48delA
ISCN -
DB-ID LHCGR_000004
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHCGR NM_000233.3 -/. - c.681-48del r.(=) p.(=)
STON1-GTF2A1L NM_001198593.1 -/. - c.3441+27179del r.(=) p.(=)
GTF2A1L NM_006872.3 -/. - c.*19417del r.(?) p.(=)
STON1 NM_006873.3 -/. - c.*103557del r.(?) p.(=)


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