Variant #0000061286 (NC_000012.11:g.50045947T>G, NM_175736.4:c.1372A>C (FMNL3))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.50045947T>G
DNA change (hg38) g.49652164T>G
Published as -
ISCN -
DB-ID FMNL3_000002 See all 2 reported entries
Variant remarks cDNA expression cloning no overexpression difference axonal outgrowth or arborization mouse primary hippocampal neurons overexpressing with/without p.Phe38Leu
Reference PubMed: Kumar 2015, PubMed: Kumar 2015
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-03-13 21:51:08 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FMNL3 NM_175736.4 -?/. 14 c.1372A>C r.(?) p.Ile458Leu


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