Variant #0000850151 (NC_000003.11:g.138664845G>T, NM_023067.3:c.720C>A (FOXL2))

Chromosome 3
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.138664845G>T
DNA change (hg38) -
Published as FOXL2(NM_023067.4):c.720C>A (p.G240=)
ISCN -
DB-ID C3orf72_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C3orf72 NM_001040061.2 -?/. - c.-1362G>T r.(?) p.(=)
FOXL2 NM_023067.3 -?/. - c.720C>A r.(?) p.(Gly240=)


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