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Items: 29

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC36A1
(S24C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC36A1
(S44R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SLC36A1
(R30L +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SLC36A1
(R107H +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SLC36A1
(R133W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(R133Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(R141G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(R113C +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SLC36A1
(T150A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
Duplication
(nonsense)
Autism
GUncertain significance
SLC36A1
(T185M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(I159M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(I191V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SLC36A1
(Y236C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(H220N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(L274P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(S277C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SLC36A1
(F317I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(F323L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(F362L +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SLC36A1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SLC36A1
(H369R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(R395C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(L413F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(P403S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(Y425C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
(Q433R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC36A1
Copy number loss
not provided
GUncertain significance
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