Variant #0000929567 (NC_000009.11:g.139091656C>T, NM_178138.4:c.322G>A (LHX3))

Chromosome 9
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.139091656C>T
DNA change (hg38) -
Published as LHX3(NM_014564.3):c.337G>A (p.(Asp113Asn))
ISCN -
DB-ID LHX3_000036
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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHX3 NM_014564.3 ?/. - c.337G>A r.(?) p.(Asp113Asn)
LHX3 NM_178138.4 ?/. - c.322G>A r.(?) p.(Asp108Asn)


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