U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRPH, TROAP-AS1
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
PRPH, TROAP-AS1
Single nucleotide variant
(5 prime UTR variant)
not provided
Gnot provided
PRPH, TROAP-AS1
(R9Q)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 1
+1 more
GBenign
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GBenign/Likely benign
PRPH, TROAP-AS1
(R77fs)
Deletion
(non-coding transcript variant +1 more)
Amyotrophic lateral sclerosis, susceptibility to
Grisk factor
PRPH, TROAP-AS1
(R133P)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
PRPH, TROAP-AS1
(D141Y)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
TROAP-AS1, PRPH
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
PRPH, TROAP-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
PRPH, TROAP-AS1
(A277T)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GBenign/Likely benign
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
PRPH-related disorder
+1 more
GBenign/Likely benign
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
LOC124629354, PRPH
+1 more
(E370K)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely benign
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
Gnot provided
LOC124629354, PRPH
+1 more
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
PRPH, TROAP-AS1
Single nucleotide variant
(intron variant)
not provided
GBenign
PRPH, TROAP-AS1
Duplication
(intron variant)
not provided
Gnot provided
PRPH, TROAP-AS1
Single nucleotide variant
(3 prime UTR variant)
not provided
Gnot provided
Format
Items per page
Sort by
Choose Destination