U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLS2, SPRYD4
(Q286L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(M128R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(R320Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(L233R)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(R166C)
Single nucleotide variant
(5 prime UTR variant +3 more)
not specified
GUncertain significance
GLS2, SPRYD4
(R207Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
GLS2, SPRYD4
(K253Q)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(N252K)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(M39V +1 more)
Single nucleotide variant
(synonymous variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(R206W +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(G254E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(I228T)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(G325S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, LOC130008086
(A6V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(A155T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(G300R +1 more)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
GLS2, SPRYD4
(V97I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
(L305F +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GLS2, SPRYD4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
GLS2, SPRYD4
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GLikely benign
Format
Items per page
Sort by
Choose Destination