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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP3K5
(I1250V)
Single nucleotide variant
(missense variant)
not provided
GBenign
MAP3K5
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MAP3K5
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MAP3K5
Single nucleotide variant
(intron variant)
not provided
GBenign
MAP3K5
Single nucleotide variant
(intron variant)
not provided
GBenign
MAP3K5, MAP3K5-AS1
Single nucleotide variant
(intron variant)
not provided
GBenign
MAP3K5
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LOC129997241, MAP3K5
Single nucleotide variant
(synonymous variant)
not provided
GBenign
AHI1, BCLAF1
+12 more
Deletion
Peroxisome biogenesis disorder 9B
GPathogenic
BCLAF1, IFNGR1
+8 more
Deletion
Immunodeficiency 27A
GPathogenic
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