Variant #0000279086 (NC_000001.10:g.180235728C>T, NM_033343.3:c.450C>T (LHX4))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.180235728C>T
DNA change (hg38) g.180266593C>T
Published as LHX4(NM_033343.3):c.450C>T (p.(Asn150=)), LHX4(NM_033343.4):c.450C>T (p.N150=)
ISCN -
DB-ID LHX4_000009 See all 3 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) 0.01886 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 2018-01-15 20:58:59 +01:00 (CET)
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.450C>T r.(?) p.(Asn150=)


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