Variant #0000605573 (NC_000001.10:g.240370684C>A, NM_020066.4:c.2572C>A (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.240370684C>A
DNA change (hg38) g.240207384C>A
Published as FMN2(NM_001305424.1):c.2584C>A (p.P862T), FMN2(NM_020066.4):c.2572C>A (p.(Pro858Thr))
ISCN -
DB-ID FMN2_000051 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) 0.00108 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +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.2572C>A r.(?) p.(Pro858Thr)


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