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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126807485, SEMA6A
(R237G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(R677Q +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(V633L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(P618H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(R713W +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(H642Q +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LOC126807485, SEMA6A
(G229A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(W606R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A, SEMA6A-AS1
(S591L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA6A
Copy number loss
not provided
GUncertain significance
SEMA6A
Copy number gain
not provided
GUncertain significance
LOC126807485, SEMA6A
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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