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Links from Gene

Items: 68

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM171B, LOC129935235
(V8F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(P590L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(N245D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(D691A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(V214I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(C382Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(R288H)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FAM171B
(P276L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(I271V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(P803Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(V80A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(T67A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(Q553K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(G335E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(K266Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(R450G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(V18L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(V569I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(S779L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AAMP, ABCA12
+208 more
Copy number gain
See cases
GPathogenic
FAM171B
(R820H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(N464S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(L202S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(T136I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(L265P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(A291S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(N488S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FAM171B
(M296V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(P494T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(Q474K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(T796S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(N313D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(R579Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(E61K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FAM171B
(Y623F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CALCRL, FAM171B
+3 more
Copy number gain
not provided
GUncertain significance
ANKAR, ANKRD44
+48 more
Copy number loss
not provided
GPathogenic
ABCA12, ABCB11
+1216 more
Copy number gain
Mosaic trisomy 2
GPathogenic
ABI2, ACADL
+127 more
Copy number loss
Chromosome 2q32-q33 deletion syndrome
GPathogenic
AGPS, ANKAR
+217 more
Copy number gain
not specified
GPathogenic
AAMP, ABCA12
+384 more
Copy number gain
See cases
GPathogenic
AGPS, ANKAR
+86 more
Copy number loss
not provided
GPathogenic
CASP8, CAVIN2
+233 more
Copy number gain
not provided
GPathogenic
FAM171B
(P250S)
Single nucleotide variant
(missense variant)
not provided
GBenign
FAM171B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FAM171B
(R95H)
Single nucleotide variant
(missense variant)
not provided
GBenign
FAM171B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FAM171B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FAM171B
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FAM171B, ITGAV
Copy number gain
not provided
GUncertain significance
ABCB11, AGPS
+125 more
Copy number loss
not provided
GPathogenic
CALCRL, FAM171B
+5 more
Copy number gain
not provided
GUncertain significance
CALCRL, FAM171B
+4 more
Copy number loss
not provided
GUncertain significance
CALCRL, FAM171B
+5 more
Deletion
Neurodevelopmental disorder
GPathogenic
RGPD4, RGPD5
+1214 more
Copy number gain
See cases
GPathogenic
IL1F10, IL1R1
+1214 more
Copy number gain
See cases
GPathogenic
AGPS, ANKAR
+62 more
Copy number loss
See cases
GPathogenic
AGPS, ANKAR
+377 more
Copy number loss
See cases
GPathogenic
ANKAR, ASDURF
+312 more
Copy number loss
See cases
GPathogenic
INPP1, ITGA4
+1097 more
Copy number gain
See cases
GPathogenic
ANKAR, ASDURF
+191 more
Copy number loss
See cases
GPathogenic
CALCRL, CALCRL-AS1
+88 more
Copy number loss
See cases
GPathogenic
AGPS, ATF2
+307 more
Copy number loss
See cases
GPathogenic
AGPS, ATF2
+417 more
Copy number loss
See cases
GPathogenic
ANKAR, ANKRD44
+329 more
Copy number loss
See cases
GPathogenic
ANKAR, ANKRD44
+430 more
Copy number loss
See cases
GPathogenic
LOC126806416, LOC126806417
+591 more
Copy number loss
See cases
GPathogenic
LOC129935164, LOC129935165
+697 more
Copy number loss
See cases
GPathogenic
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