Variant #0000558958 (NC_000016.9:g.70513576T>A, NM_015386.2:c.*1337A>T (COG4))

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.70513576T>A
DNA change (hg38) g.70479673T>A
Published as FUK(NM_145059.3):c.3248T>A (p.F1083Y)
ISCN -
DB-ID FUK_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) 0.00025 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG4 NM_015386.2 -?/. - c.*1337A>T r.(=) p.(=)
FUK NM_145059.2 -?/. - c.3248T>A r.(?) p.(Phe1083Tyr)


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