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Links from Gene

Items: 47

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDXP-DT, SH3BP1
(R121G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P578R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P577H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R390C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(M418K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R408Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P521Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(E294K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(T266I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P689S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(Q634R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R633H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R632Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R632W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P578S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P577R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(S550R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(V504M)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(A465S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P393R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R380Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
PDXP-DT, SH3BP1
(R633C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(T467S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(A248S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(L592F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(A379P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P126A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(V297I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R287Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(S536P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(S329L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(S695C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(V449A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(A589D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(T266A)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
PDXP-DT, SH3BP1
(V504A)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R121K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R567H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P393A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(S581F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(E284K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(R572Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P568Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(P176L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
PDXP-DT, SH3BP1
(L444R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PDXP-DT, SH3BP1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
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