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Links from Gene

Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862878, SUGP2
(E182K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R140Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(L216V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(D334N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(I333V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
LOC126862878, SUGP2
(D331E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R189Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(G174E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R132C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R48I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(C107R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R311G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(L42I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R62S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R214Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(E66D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
LOC126862878, SUGP2
(E185D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(P276L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(I255K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(S329N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(R322Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(T354A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862878, SUGP2
(S96R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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