Variant #0000913120 (NC_000009.11:g.139089389T>G, NM_178138.4:c.976A>C (LHX3))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139089389T>G
DNA change (hg38) -
Published as LHX3(NM_014564.3):c.991A>C (p.(Ser331Arg))
ISCN -
DB-ID LHX3_000035
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHX3 NM_014564.3 -?/. - c.991A>C r.(?) p.(Ser331Arg)
LHX3 NM_178138.4 -?/. - c.976A>C r.(?) p.(Ser326Arg)


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