Variant #0000268970 (NC_000015.9:g.31197584G>A, NM_014967.4:c.718G>A (FAN1))

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.31197584G>A
DNA change (hg38) g.30905381G>A
Published as FAN1(NM_014967.5):c.718G>A (p.E240K)
ISCN -
DB-ID FAN1_000005 See all 2 reported entries
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) 0.00346 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAN1 NM_014967.4 -?/. - c.718G>A r.(?) p.(Glu240Lys)
MTMR10 NM_017762.2 -?/. - c.*36089C>T r.(=) p.(=)


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