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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM132E
(H28Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM132E
(R127Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM132E
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TMEM132E
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TMEM132E
(R767Q)
Single nucleotide variant
(missense variant)
TMEM132E-related condition
+2 more
GLikely benign
TMEM132E
(P862A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM132E
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TMEM132E
Duplication
(inframe_insertion)
not provided
GUncertain significance
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