Variant #0000290958 (NC_000001.10:g.226125260C>T, LEFTY2(NM_003240.3):c.982G>A)

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.226125260C>T
DNA change (hg38) g.225937560C>T
Published as LEFTY2(NM_003240.4):c.982G>A (p.V328I)
ISCN -
DB-ID LEFTY2_000001 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00943 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LEFTY2 NM_003240.3 -/. - c.982G>A r.(?) p.(Val328Ile)