Variant #0000611984 (NC_000009.11:g.139089553C>T, NM_178138.4:c.812G>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.139089553C>T
DNA change (hg38) g.136197707C>T
Published as LHX3(NM_014564.3):c.827G>A (p.(Gly276Asp))
ISCN -
DB-ID LHX3_000017
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) 4.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHX3 NM_014564.3 ?/. - c.827G>A r.(?) p.(Gly276Asp)
LHX3 NM_178138.4 ?/. - c.812G>A r.(?) p.(Gly271Asp)


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