chr3:138946051:>AGCTGCTGCAGCCGCAGCTGCTGCAGCCGC Detail (hg38) (FOXL2)

Information

Genome

Assembly Position
hg19 chr3:138,664,893-138,664,893 
hg38 chr3:138,946,051-138,946,051

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000648323.1:c.671_672insGCGGCTGCAGCAGCTGCGGCTGCAGCAGCT ENST00000648323.1:p.Ala225_Ala234dup
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 605597 OMIM
HGNC 1092 HGNC
Ensembl ENSG00000183770 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 Blepharophimosis syndrome type 2 NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs387906322 dbSNP
Genome
hg38
Position
chr3:138,946,051-138,946,051
Variant Type
snv
Reference Allele
-
Alternative Allele
AGCTGCTGCAGCCGCAGCTGCTGCAGCCGC
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