Variant #0000559214 (NC_000016.9:g.7759112C>A, NM_001142333.1:c.969C>A (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.7759112C>A
DNA change (hg38) g.7709110C>A
Published as RBFOX1(NM_001142333.1):c.969C>A (p.(=)), RBFOX1(NM_001364800.1):c.1103C>A (p.P368Q)
ISCN -
DB-ID RBFOX1_000029 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) 5.0E-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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBFOX1 NM_001142333.1 -?/. - c.969C>A r.(?) p.(Pro323=)
RBFOX1 NM_018723.3 -?/. - c.1050C>A r.(?) p.(Pro350=)


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