Variant #0001041358 (NC_000016.9:g.7568263C>T, NM_001142333.1:c.142C>T (RBFOX1))

Chromosome 16
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.7568263C>T
DNA change (hg38) -
Published as RBFOX1(NM_018723.4):c.142C>T (p.(Pro48Ser))
ISCN -
DB-ID RBFOX1_000006 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) 0.00063 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 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     
RBFOX1 NM_001142333.1 -?/. - c.142C>T r.(?) p.(Pro48Ser)
RBFOX1 NM_018723.3 -?/. - c.142C>T r.(?) p.(Pro48Ser)


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