Variant #0000981523 (NC_000015.9:g.91424702T>G, NM_002569.2:c.1979T>G (FURIN))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.91424702T>G
DNA change (hg38) -
Published as FURIN(NM_002569.4):c.1979T>G (p.(Leu660Arg))
ISCN -
DB-ID FES_000013
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FES NM_002005.3 ?/. - c.-3082T>G r.(?) p.(=)
FURIN NM_002569.2 ?/. - c.1979T>G r.(?) p.(Leu660Arg)


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