U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 29

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFNAR1
Deletion
not provided
GLikely pathogenic
IFNAR1
Single nucleotide variant
(stop lost +2 more)
Immunodeficiency 106, susceptibility to viral infections
GUncertain significance
IFNAR1
Deletion
(3 prime UTR variant +2 more)
Immunodeficiency 106, susceptibility to viral infections
GUncertain significance
IFNAR1
Deletion
(frameshift variant +2 more)
Immunodeficiency 106, susceptibility to viral infections
GUncertain significance
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(intron variant)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
(S22A)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1
Deletion
Immunodeficiency 106, susceptibility to viral infections
GPathogenic
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
LOC119230225, IFNAR1
(V4I)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
Single nucleotide variant
(intron variant)
not provided
GLikely benign
IFNAR1, LOC119230225
(T10fs)
Deletion
(frameshift variant +2 more)
not provided
GPathogenic
IFNAR1, LOC119230225
(A17V)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
(L5R)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(intron variant)
not provided
GLikely benign
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1, LOC119230225
(L6P)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
(V16M)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
(L11V)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
Microsatellite
(inframe_deletion +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
(T10A)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GConflicting classifications of pathogenicity
IFNAR1, LOC119230225
(W19G)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
IFNAR1, LOC119230225
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
IFNAR1
(W277*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
Format
Items per page
Sort by
Choose Destination