Variant #0000725386 (NC_000015.9:g.91423510G>C, NC_000015.9(NM_002569.2):c.1556+7G>C (FURIN))

Chromosome 15
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.91423510G>C
DNA change (hg38) -
Published as FURIN(NM_001289823.1):c.1556+7G>C (p.(=))
ISCN -
DB-ID FES_000008
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) 0.0004 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FES NM_002005.3 -?/. - c.-4274G>C r.(?) p.(=)
FURIN NM_002569.2 -?/. - c.1556+7G>C r.(=) p.(=)


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