Variant #0000530027 (NC_000007.13:g.100183710A>G, NM_001163499.1:c.-3554A>G (FBXO24))

Chromosome 7
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.100183710A>G
DNA change (hg38) g.100586087A>G
Published as LRCH4(NM_002319.3):c.14T>C (p.(Val5Ala))
ISCN -
DB-ID FBXO24_000001
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) 3.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO24 NM_001163499.1 -?/. - c.-3554A>G r.(?) p.(=)
LRCH4 NM_002319.3 -?/. - c.14T>C r.(?) p.(Val5Ala)


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