Variant #0000290969 (NC_000002.11:g.48982622C>G, NC_000002.11(NM_000233.3):c.161+28G>C (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.48982622C>G
DNA change (hg38) g.48755483C>G
Published as LHCGR(NM_000233.3):c.161+28G>C
ISCN -
DB-ID LHCGR_000006
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) 0.18733 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 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.161+28G>C r.(=) p.(=)
STON1-GTF2A1L NM_001198593.1 -/. - c.3442-20797C>G r.(=) p.(=)
GTF2A1L NM_006872.3 -/. - c.*76041C>G r.(=) p.(=)
STON1 NM_006873.3 -/. - c.*160181C>G r.(=) p.(=)


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