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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRMT1
Single nucleotide variant
(synonymous variant)
Intellectual developmental disorder, autosomal recessive 68
GUncertain significance
TRMT1
(L201P +3 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 68
GUncertain significance
TRMT1
(C126fs +3 more)
Microsatellite
(frameshift variant)
Intellectual developmental disorder, autosomal recessive 68
GLikely pathogenic
TRMT1
(G99S +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
TRMT1
Single nucleotide variant
(intron variant)
Intellectual developmental disorder, autosomal recessive 68
GUncertain significance
TRMT1
(T11A +2 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal recessive 68
GUncertain significance
TRMT1
(R159W +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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