chr1:209790667:GTCCAGCAGCTTGCTAGTG>T Detail (hg38) (IRF6)

Information

Genome

Assembly Position
hg19 chr1:209,964,012-209,964,030 View the variant detail on this assembly version.
hg38 chr1:209,790,667-209,790,685

HGVS

Type Transcript Protein
RefSeq NM_006147.3:c.870_888delinsA NP_006138.1:p.Phe290_Asp296delinsLeu
NM_001206696.1:c.585_603delinsA NP_001193625.1:p.Phe195_Asp201delinsLeu
Ensemble ENST00000367021.8:c.870_888delinsA ENST00000367021.8:p.Phe290_Asp296delinsLeu
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 607199 OMIM
HGNC 6121 HGNC
Ensembl ENSG00000117595 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
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2002-10-01 no assertion criteria provided Van der Woude syndrome 1 germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.575 Van der Woude syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006147.4(IRF6):c.870_888delinsA (p.Phe290_Asp296delinsLeu) AND Van der Woude syndrome 1 ClinVar Detail
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
rs587776569 dbSNP
Genome
hg38
Position
chr1:209,790,667-209,790,685
Variant Type
snv
Reference Allele
GTCCAGCAGCTTGCTAGTG
Alternative Allele
T
Genome browser