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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862088, TRPM1
Single nucleotide variant
(splice donor variant)
Congenital stationary night blindness 1C
GLikely pathogenic
TRPM1
(V1014fs +2 more)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
TRPM1
(R877* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
TRPM1
(Y649* +2 more)
Single nucleotide variant
(nonsense)
Congenital stationary night blindness 1C
GPathogenic
TRPM1
(R673* +2 more)
Single nucleotide variant
(nonsense)
Congenital stationary night blindness 1C
+1 more
GPathogenic/Likely pathogenic
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