Variant #0000858825 (NC_000003.11:g.138664931G>C, NM_023067.3:c.634C>G (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.138664931G>C
DNA change (hg38) -
Published as FOXL2(NM_023067.4):c.634C>G (p.P212A)
ISCN -
DB-ID C3orf72_000010
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) 0.00014 View details
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 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C3orf72 NM_001040061.2 ?/. - c.-1276G>C r.(?) p.(=)
FOXL2 NM_023067.3 ?/. - c.634C>G r.(?) p.(Pro212Ala)


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