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Links from Gene

Items: 1 to 100 of 736

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DGAT1
Deletion
Congenital diarrhea 7 with exudative enteropathy
GUncertain significance
DGAT1
(V407fs)
Duplication
(frameshift variant)
DGAT1-related disorder
GLikely pathogenic
DGAT1, LOC130001386
(M1V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DGAT1
(R222K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DGAT1
(S307P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1
Deletion
not provided
GLikely pathogenic
DGAT1
Deletion
not provided
GPathogenic
ADCK5, ARHGAP39
+44 more
Copy number gain
not provided
GUncertain significance
DGAT1
(R272G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1
(S270P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1
(W217C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1
(P392L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1, LOC130001383
(H343Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DGAT1
(L279P)
Single nucleotide variant
(missense variant)
Congenital diarrhea 7 with exudative enteropathy
GUncertain significance
ADCK5, ARHGAP39
+63 more
Copy number gain
not specified
GUncertain significance
AARD, ABRA
+665 more
Copy number gain
not specified
GPathogenic
DGAT1
Single nucleotide variant
(synonymous variant)
DGAT1-related disorder
GLikely benign
NRBP2, NSMCE2
+173 more
Copy number gain
not provided
GPathogenic
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, LOC130001386
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
(E161Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Insertion
(intron variant)
not provided
GLikely benign
DGAT1
Microsatellite
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
(W384*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
DGAT1
Deletion
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001386
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Deletion
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, MIR6848
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Duplication
(intron variant)
not provided
GBenign
DGAT1, LOC130001383
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001386
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001386
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, LOC130001383
(Y339F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DGAT1, MIR6848
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
DGAT1, LOC130001383
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, LOC130001386
(P24fs)
Deletion
(frameshift variant)
not provided
GPathogenic
DGAT1
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DGAT1, MIR6848
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
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