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Links from Gene

Items: 28

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGAP19, ARHGAP19-SLIT1
(F308L +1 more)
Single nucleotide variant
(non-coding transcript variant +2 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(M182I +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(L158F +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(I129T +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(E10A)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(K48T +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(T369M +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(H292Y +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
ARHGAP19, ARHGAP19-SLIT1
(V351I +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(S16C)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(H194Q +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(T474M +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(R214W +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(S115F +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(R106Q +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(A389T +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(E10Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(I384T +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(R231H +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(A329S +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(R407L +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(S139G +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(L70P +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(G81V +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(L291F +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(K221E +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(N55S +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
ARHGAP19, ARHGAP19-SLIT1
(T336A +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
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