Variant #0000689455 (NC_000005.9:g.147774426T>C, NM_030793.3:c.87T>C (FBXO38))

Chromosome 5
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.147774426T>C
DNA change (hg38) -
Published as FBXO38(NM_030793.5):c.87T>C (p.Y29=), FBXO38(NM_205836.2):c.87T>C (p.Y29=)
ISCN -
DB-ID FBXO38_000001 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) 0.00285 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO38 NM_030793.3 -?/. - c.87T>C r.(?) p.(Tyr29=)
FBXO38 NM_030793.4 -?/. - c.87T>C r.(?) p.(Tyr29=)


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