Variant #0001015375 (NC_000016.9:g.2506800G>A, NM_025108.2:c.-3346G>A (C16orf59))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2506800G>A
DNA change (hg38) -
Published as CCNF(NM_001761.3):c.2140G>A (p.V714M)
ISCN -
DB-ID CCNF_000004
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) 0.00975 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNF NM_001761.2 -/. - c.2140G>A r.(?) p.(Val714Met)
C16orf59 NM_025108.2 -/. - c.-3346G>A r.(?) p.(=)


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