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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMMECR1L, BIN1
+254 more
Copy number loss
See cases
GPathogenic
ACMSD, AMER3
+391 more
Copy number loss
See cases
GPathogenic
NIFK, NIFK-AS1
(R288Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NIFK, NIFK-AS1
(K257E)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(Q248fs)
Microsatellite
(non-coding transcript variant +1 more)
not provided
GLikely benign
NIFK, NIFK-AS1
(R245Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(P239L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(S218A)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(R211L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(R211H)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(R211C)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
NIFK, NIFK-AS1
(T203M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
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