Variant #0000990583 (NC_000001.10:g.180243706C>A, NM_033343.3:c.1165C>A (LHX4))

Chromosome 1
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.180243706C>A
DNA change (hg38) -
Published as LHX4(NM_033343.3):c.1165C>A (p.(Pro389Thr)), LHX4(NM_033343.4):c.1165C>A (p.P389T)
ISCN -
DB-ID LHX4_000015 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) 0.00028 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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHX4 NM_033343.3 -?/. - c.1165C>A r.(?) p.(Pro389Thr)


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