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Links from Gene

Items: 1 to 100 of 1419

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPA1
Single nucleotide variant
(intron variant)
not specified
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
OPA1-related condition
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
OPA1-related condition
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
OPA1-related condition
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
OPA1-related condition
GLikely benign
OPA1
(T488A +9 more)
Single nucleotide variant
(missense variant)
OPA1-related condition
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
OPA1-related condition
GLikely benign
OPA1
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
OPA1
(Q51R)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(S130N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(Q622R +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(V581I +9 more)
Inversion
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1, OPA1-AS1
(R158G +5 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
OPA1
(E768del +9 more)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
OPA1
(R503G +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1, OPA1-AS1
(R194G +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC126806913, OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(H163R +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(V792A +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
OPA1, OPA1-AS1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(A937V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(N468S +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(D168H +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(N475S +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(K721R +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(D793V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
OPA1
(D168E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
(S727G +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(E750D +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(S39N)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
OPA1
(M561V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(D921A +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(I40V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
(S472N +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1, OPA1-AS1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Deletion
(intron variant)
not provided
GLikely benign
OPA1
Deletion
(intron variant)
not provided
GLikely benign
OPA1
Duplication
(intron variant)
not provided
GUncertain significance
OPA1
(S721N +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1-AS1, OPA1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(G352S +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(I504F +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(M197I +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1, OPA1-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
OPA1
(P29Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
OPA1
(L967V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(T777I +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1, OPA1-AS1
(T36A +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
(A273V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
Deletion
(intron variant)
not provided
GLikely benign
OPA1
Deletion
(frameshift variant)
not provided
GPathogenic
OPA1, OPA1-AS1
(Q234P +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
OPA1
(A532G +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(Q606H +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(K302fs +9 more)
Deletion
(frameshift variant)
not provided
GPathogenic
OPA1, OPA1-AS1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
OPA1
(K906* +9 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
OPA1, OPA1-AS1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
OPA1
(D689G +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(S611A +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(V13G)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
OPA1
(R588Q +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
OPA1
(K32Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
OPA1
(T161fs +9 more)
Duplication
(frameshift variant)
not provided
GPathogenic
OPA1
(A293P +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
OPA1
(I735V +9 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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