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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLX6, DLX6-AS1
(G13S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(Q42H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(P70S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(H87Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(S107F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
+1 more
(A136E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(D144H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(Q228H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(D236E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
(S248L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DLX6, DLX6-AS1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
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