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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIM37
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign/Likely benign
TRIM37
(S801P +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TRIM37
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
TRIM37
(N747S +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TRIM37
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign/Likely benign
TRIM37
(R640H +5 more)
Single nucleotide variant
(missense variant +1 more)
Mulibrey nanism syndrome
+1 more
GConflicting classifications of pathogenicity
TRIM37
(E483K +5 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
TRIM37
(R471* +5 more)
Single nucleotide variant
(nonsense +1 more)
Mulibrey nanism syndrome
+1 more
GPathogenic
TRIM37
(S339T +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TRIM37
(N317S +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
TRIM37
(S287N +4 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely pathogenic
TRIM37
(S233N +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
TRIM37
Single nucleotide variant
(synonymous variant +2 more)
not provided
GUncertain significance
TRIM37
(A133V +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GBenign/Likely benign
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