Variant #0000518066 (NC_000003.11:g.138664847C>T, NM_023067.3:c.718G>A (FOXL2))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.138664847C>T
DNA change (hg38) g.138946005C>T
Published as FOXL2(NM_023067.3):c.718G>A (p.(Gly240Ser)), FOXL2(NM_023067.4):c.718G>A (p.G240S)
ISCN -
DB-ID FOXL2_000002 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) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C3orf72 NM_001040061.2 ?/. - c.-1360C>T r.(?) p.(=)
FOXL2 NM_023067.3 ?/. - c.718G>A r.(?) p.(Gly240Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.