Variant #0000537142 (NC_000009.11:g.139089190A>G, NM_178138.4:c.1175T>C (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.139089190A>G
DNA change (hg38) g.136197344A>G
Published as LHX3(NM_014564.3):c.1190T>C (p.(Val397Ala)), LHX3(NM_014564.5):c.1190T>C (p.V397A)
ISCN -
DB-ID LHX3_000011 See all 2 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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
LHX3 NM_014564.3 ?/. - c.1190T>C r.(?) p.(Val397Ala)
LHX3 NM_178138.4 ?/. - c.1175T>C r.(?) p.(Val392Ala)


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