Variant #0000504356 (NC_000001.10:g.180199701G>A, NM_033343.3:c.37G>A (LHX4))

Chromosome 1
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.180199701G>A
DNA change (hg38) g.180230566G>A
Published as LHX4(NM_033343.3):c.37G>A (p.(Val13Ile)), LHX4(NM_033343.4):c.37G>A (p.V13I)
ISCN -
DB-ID LHX4_000016 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) 0.00019 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     
LHX4 NM_033343.3 ?/. - c.37G>A r.(?) p.(Val13Ile)


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