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NM_001347928.2 - NP_001334857.1
NM_001098629.3 - NP_001092099.1 (MANE)
NM_001098630.3 - NP_001092100.1
NM_001242452.3 - NP_001229381.1
NM_032643.5 - NP_116032.1
NM_001098627.4 - NP_001092097.2
NM_001364314.2 - NP_001351243.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
7
Location
Chr7:128,936,532-128,950,538
LOEUF
0.595
Variant filter
By data sources
ClinVar
Pathogenic/ Likely pa...
Risk factor
Drug response
Association
Affect
VUS
Benign/Likely benign
Others
GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
Others
Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
IRF5
interferon regulatory factor 5
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