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Items: 41

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SHMT1
(P439R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(L474R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(L474F +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
GUncertain significance
SHMT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SHMT1
(A321V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(E408D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(T400I +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SHMT1
(R273C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(R264W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(R358W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(A340S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SHMT1
(I310T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(E206Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(E340Q +2 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SHMT1
(V312I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(I171V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
(G299V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
Single nucleotide variant
(intron variant)
not provided
GBenign
SHMT1
(R263Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(T120I +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SHMT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SHMT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SHMT1
(A237V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SHMT1
(G234R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(G84E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(K216R +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
SHMT1
(R213W +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
SHMT1
(R53H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(D18E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SHMT1
(R137H)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SHMT1
(V115I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
(P108S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
(K105N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
(Q97L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
(I89T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SHMT1
Single nucleotide variant
(intron variant)
not provided
GBenign
SHMT1
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
SHMT1
(M3V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SHMT1
(M1R)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GLikely benign
SHMT1
(M1K)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GBenign
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