Variant #0000605575 (NC_000001.10:g.240371000_240371001insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG, NM_020066.4:c.2888_2889insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG (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.240371000_240371001insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG
DNA change (hg38) g.240207700_240207701insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG
Published as FMN2(NM_020066.4):c.2886_2887insGGAATACCTCCTCCACCCCCTCTACCCGGAGCG (p.(Pro955_Pro965dup))
ISCN -
DB-ID FMN2_000079
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 2019-12-04 14:54:23 +01:00 (CET)
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     
FMN2 NM_020066.4 -?/. - c.2888_2889insAATACCTCCTCCACCCCCTCTACCCGGAGCGGG r.(?) p.(Pro955_Pro965dup)


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