U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 46

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC38A9
(G272R +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(K321R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(I210T +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(S261C +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(S133T +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(I217M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(I90T +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(R48W +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(R73Q +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(I464V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(I411V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
SLC38A9
(G409S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(G468S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(R400C +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(N19D +1 more)
Single nucleotide variant
(5 prime UTR variant +3 more)
not specified
GUncertain significance
SLC38A9
(T279I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(M335R +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(E349K +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ACTBL2, ANKRD55
+35 more
Copy number loss
not specified
GLikely pathogenic
SLC38A9
(R11W)
Single nucleotide variant
(missense variant +1 more)
EBV-positive nodal T- and NK-cell lymphoma
GLikely benign
SLC38A9
(V428M +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ANKRD55, ARL15
+23 more
Deletion
not provided
GPathogenic
SLC38A9
(R9K)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SLC38A9
(G88S +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(S440P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC38A9
(L136P +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(L57F +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SLC38A9
(Y136H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(I547V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(M124T +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(T123I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC38A9
(V482I +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
SLC38A9
(T298S +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ANKRD55, CCNO
+7 more
Copy number gain
not provided
GUncertain significance
C5orf24, C5orf34
+600 more
Deletion
Neurodevelopmental disorder
GUncertain significance
MTREX, PLPP1
+1 more
Copy number gain
not provided
GLikely benign
DHFR, DHX29
+738 more
Copy number loss
See cases
GPathogenic
ABLIM3, ACOT12
+870 more
Copy number gain
See cases
GPathogenic
ABLIM3, ACOT12
+870 more
Copy number gain
See cases
GPathogenic
SLC38A9, SNX18
+12 more
Copy number loss
Abnormal esophagus morphology
GLikely benign
CCNO, CCNO-DT
+35 more
Copy number gain
See cases
GUncertain significance
ACTBL2, ADAMTS12
+1445 more
Copy number gain
See cases
GPathogenic
ANKRD55, ARL15
+125 more
Copy number gain
See cases
GUncertain significance
LINC02057, LINC02101
+518 more
Copy number gain
See cases
GPathogenic
ARL15, CCNO
+96 more
Copy number loss
See cases
GPathogenic
ACTBL2, ANKRD55
+269 more
Copy number loss
See cases
GPathogenic
Format
Items per page
Sort by
Choose Destination