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Items: 61

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM106B
(S4C)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
TMEM106B
(S13G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
(M26V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
TMEM106B
(D39V)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
TMEM106B
(G40A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TMEM106B
(G43E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(G43A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(Y50C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
TMEM106B
Duplication
(intron variant)
not provided
GBenign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
(V98M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
(D122N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
(S134N)
Single nucleotide variant
(missense variant)
not provided
GBenign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
(R140H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Duplication
(intron variant)
not provided
GBenign
TMEM106B
(N148S)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
TMEM106B
(E161K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
(L181F)
Single nucleotide variant
(missense variant)
not provided
GBenign
TMEM106B
(T185G)
Indel
(missense variant)
not provided
GUncertain significance
TMEM106B
(T185S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
TMEM106B
(I187V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(M192V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(M192K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(M192I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Deletion
(intron variant)
not provided
GBenign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TMEM106B
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TMEM106B
Inversion
(intron variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TMEM106B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
TMEM106B
(L261M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(Y266C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
(L270F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TMEM106B
Deletion
not provided
GLikely benign
TMEM106B
Deletion
not provided
GUncertain significance
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