Variant #0000858824 (NC_000003.11:g.138664893_138664895del, NM_023067.3:c.672_674del (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.138664893_138664895del
DNA change (hg38) -
Published as FOXL2(NM_023067.4):c.672_674delAGC (p.A234del)
ISCN -
DB-ID C3orf72_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +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.-1314_-1312del r.(?) p.(=)
FOXL2 NM_023067.3 ?/. - c.672_674del r.(?) p.(Ala234del)


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