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Links from Gene

Items: 66

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRM4
(S583L +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(P38L)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(G426E +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R78W)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(G140D)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(R517C +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R687C +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(T134I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(R129C +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(M27I)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(V905I +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(H136Y +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(E63D +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(Q38R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(G137S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(A589V +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(A848V +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R88L)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(M528V +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(T512M +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(T650M +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(N782S +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(D306N +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R385C +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R470H +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R258H +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(I336T +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(N305K +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R125W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(P34S)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(D479N +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARMC12, BRPF3
+94 more
Duplication
not provided
GUncertain significance
ABHD16A, AGER
+172 more
Duplication
Proteasome-associated autoinflammatory syndrome 1
GUncertain significance
GRM4
(G68V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(T203M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(V263M +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(Q641R +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(T142A +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(Q205P +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(I277M +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(T402M +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(N91H)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GRM4
(Y161C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(E236D +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GRM4
(E583Q +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(H254Y +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(R303H +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(N158S +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GRM4
(K645M +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GRM4
(H39Y)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ABHD16A, AGER
+117 more
Copy number gain
not provided
GLikely pathogenic
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
(R367C +5 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
Single nucleotide variant
(intron variant)
not provided
GLikely benign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
GRM4
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ERVH-3, ETV7
+427 more
Copy number gain
not provided
GPathogenic
AARS2, ABCC10
+1028 more
Copy number gain
See cases
GPathogenic
RING1, RIOK1
+1028 more
Copy number gain
See cases
GPathogenic
ILRUN-AS1, IP6K3
+2582 more
Copy number gain
See cases
GPathogenic
GRM4, LINC01016
+18 more
Copy number loss
See cases
GUncertain significance
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