Variant #0000327003 (NC_000002.11:g.48808580A>C, NM_000233.3:c.*106256T>G (LHCGR))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48808580A>C
DNA change (hg38) g.48581441A>C
Published as STON1(NM_001198595.1):c.808A>C (p.(Ser270Arg))
ISCN -
DB-ID STON1_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) 0.00123 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*106256T>G r.(=) p.(=)
STON1-GTF2A1L NM_001198593.1 ?/. - c.808A>C r.(?) p.(Ser270Arg)
GTF2A1L NM_006872.3 ?/. - c.-36434A>C r.(?) p.(=)
STON1 NM_006873.3 ?/. - c.808A>C r.(?) p.(Ser270Arg)


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