Variant #0000558428 (NC_000016.9:g.5289865G>C, NM_001142333.1:c.-780255G>C (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.5289865G>C
DNA change (hg38) g.5239864G>C
Published as RBFOX1(XM_005255378.1):c.-17-6G>C (p.(=))
ISCN -
DB-ID RBFOX1_000018
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 2019-07-18 18:22:55 +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     
RBFOX1 NM_001142333.1 -?/. - c.-780255G>C r.(?) p.(=)
RBFOX1 NM_018723.3 -?/. - c.-780255G>C r.(?) p.(=)


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