Variant #0000675772 (NC_000001.10:g.240370951_240370952insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC, NM_020066.4:c.2839_2840insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC (FMN2))

Chromosome 1
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.240370951_240370952insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC
DNA change (hg38) -
Published as FMN2(NM_001305424.1):c.2851_2852ins33 (p.P950_P951ins11)
ISCN -
DB-ID FMN2_000086
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) 0.00066 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FMN2 NM_020066.4 -?/. - c.2839_2840insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC r.(?) p.(Pro946_Pro947insLeuLeuProGlyAlaGlyIleProLeuProPro)


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