Variant #0000351242 (NC_000002.11:g.48925746C>T, NC_000002.11(NM_000233.3):c.866+8G>A (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.48925746C>T
DNA change (hg38) g.48698607C>T
Published as LHCGR(NM_000233.3):c.866+8G>A, LHCGR(NM_000233.4):c.866+8G>A, STON1-GTF2A1L(NM_001198593.2):c.3441+26927C>T
ISCN -
DB-ID LHCGR_000003 See all 3 reported entries
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) 0.7525 View details
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 2023-01-11 15:44:22 +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.866+8G>A r.(=) p.(=)
STON1-GTF2A1L NM_001198593.1 -/. - c.3441+26927C>T r.(=) p.(=)
GTF2A1L NM_006872.3 -/. - c.*19165C>T r.(=) p.(=)
STON1 NM_006873.3 -/. - c.*103305C>T r.(=) p.(=)


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