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Links from Gene

Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACMSD, CCNT2-AS1
(T257A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(G231E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(D192E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(H238R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(M208V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
Single nucleotide variant
(synonymous variant)
ACMSD-related disorder
GLikely benign
ACMSD, CCNT2-AS1
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
ACMSD, CCNT2-AS1
(G181R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ACMSD, CCNT2-AS1
(S183R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(A223T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(D212H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(M122V +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
(K217R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACMSD, CCNT2-AS1
Single nucleotide variant
(intron variant)
See cases
GUncertain significance
ACMSD, CCNT2-AS1
Duplication
(intron variant)
not provided
GLikely benign
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