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Links from Gene

Items: 1 to 100 of 207

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX15
Single nucleotide variant
(synonymous variant)
TBX15-related disorder
GLikely benign
TBX15
Duplication
not provided
GUncertain significance
TBX15
(V599M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ADAM30, HAO2
+9 more
Copy number gain
not specified
GUncertain significance
TBX15
(G51V)
Single nucleotide variant
(missense variant +1 more)
TBX15-related disorder
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
TBX15-related disorder
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant +1 more)
TBX15-related disorder
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant +1 more)
TBX15-related disorder
GLikely benign
TBX15
(T56R)
Single nucleotide variant
(missense variant +1 more)
TBX15-related disorder
GLikely benign
TBX15
(E226K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(M601L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Deletion
(intron variant)
not provided
GBenign
ADAM30, HAO2
+9 more
Copy number gain
not provided
GUncertain significance
TBX15
(D169G +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(V115A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(H376P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(P154A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(I447N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(D144V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15, WARS2
Duplication
not provided
GUncertain significance
HAO2, HSD3B1
+5 more
Deletion
PHGDH deficiency
GPathogenic
TBX15
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TBX15
(P260S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(Y412C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(F145V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(T418I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(D227E +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(I7T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(M301T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(Y359H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBX15
(S492F +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(T169I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(Y451F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(S434I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(T208N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(D22V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TBX15
(S202Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(N407S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(A424T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(A431T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
TBX15
(R248P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(D250N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
(Y557C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(Y479H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Duplication
(intron variant)
not provided
GBenign
TBX15
(H406R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
(A176S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(W103C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(R298* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
TBX15
(P345T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
(A358T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(A551V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(I165T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
(G470R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(R298Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(T275P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(T475I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(I165V +1 more)
Single nucleotide variant
(missense variant)
Pelviscapular dysplasia
+2 more
GUncertain significance
TBX15
(D169H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
Single nucleotide variant
(intron variant)
not provided
GBenign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GLikely benign
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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