Variant #0001034577 (NC_000004.11:g.54325465C>A, NM_001126328.2:c.*1609G>T (LNX1))

Chromosome 4
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.54325465C>A
DNA change (hg38) -
Published as FIP1L1(NM_030917.4):c.1638-4C>A
ISCN -
DB-ID FIP1L1_000004
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
LNX1 NM_001126328.2 -?/. - c.*1609G>T r.(=) p.(=)
FIP1L1 NM_030917.3 -?/. - c.1638-4C>A r.spl? p.?


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