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Links from Gene

Items: 1 to 100 of 821

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALDH5A1, GPLD1
+1 more
(L70P)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(C223S)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely pathogenic
ALDH5A1
(E145G)
Single nucleotide variant
(missense variant)
ALDH5A1-related condition
GUncertain significance
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(5 prime UTR variant)
ALDH5A1-related condition
GLikely benign
ALDH5A1, LOC129995978
Duplication
(inframe_insertion)
Succinate-semialdehyde dehydrogenase deficiency
GLikely pathogenic
ALDH5A1, GPLD1
+1 more
(S35C)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
(L44fs)
Duplication
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Duplication
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Insertion
(nonsense +1 more)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, LOC129995978
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, LOC129995978
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, LOC129995978
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant +1 more)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, LOC129995978
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
(P37S)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(splice donor variant)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
(I142fs)
Deletion
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, LOC129995978
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GBenign
ALDH5A1
(R334M +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
GPLD1, LOC129995978
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(synonymous variant +1 more)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
(M305V +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
Single nucleotide variant
(splice donor variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely pathogenic
LOC129995978, ALDH5A1
+1 more
(A34V)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ACOT13, ALDH5A1
+38 more
Copy number loss
not provided
GLikely pathogenic
ALDH5A1
(G323fs +2 more)
Deletion
(frameshift variant)
ALDH5A1-related condition
GLikely pathogenic
ALDH5A1
(R302G +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1
Indel
(nonsense +1 more)
not provided
GLikely pathogenic
ALDH5A1
(A388E +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(R254K +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1, GPLD1
+1 more
(G29fs)
Deletion
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
(E152Q)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(T143fs)
Deletion
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely pathogenic
ALDH5A1
(S160F)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(Y254* +1 more)
Single nucleotide variant
(nonsense +1 more)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
(E453Q +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, GPLD1
+1 more
(T75fs)
Duplication
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
(D415fs +2 more)
Deletion
(frameshift variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely pathogenic
ALDH5A1
Single nucleotide variant
(splice donor variant +1 more)
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1
Duplication
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
Deletion
Succinate-semialdehyde dehydrogenase deficiency
GPathogenic
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
(Q43P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1
(F374L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1
(T291A +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1, LOC129995978
(A100P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1
Deletion
(nonsense)
Inborn genetic diseases
GLikely pathogenic
ALDH5A1, GPLD1
+1 more
(T75P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1, GPLD1
+1 more
(W69G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ALDH5A1, GPLD1
+1 more
(G16R)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, LOC129995978
(E114A)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, GPLD1
+1 more
(G29S)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, GPLD1
+1 more
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
(V477I +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(H180R)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(L310R +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
Single nucleotide variant
(synonymous variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1, GPLD1
+1 more
(A2V)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1, LOC129995978
(E107G)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(S517C +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
(P325A +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ALDH5A1
(R213Q)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
ALDH5A1
Single nucleotide variant
(intron variant)
Succinate-semialdehyde dehydrogenase deficiency
GLikely benign
ALDH5A1
(Q443R +2 more)
Single nucleotide variant
(missense variant)
Succinate-semialdehyde dehydrogenase deficiency
GUncertain significance
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