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Links from Gene

Items: 18

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARL5C
(L100P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARL5C
(A167T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC4A1, DCAKD
+422 more
Copy number loss
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
ARL5C
(R98W)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARL5C
(T94M)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARL5C
(E163K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARL5C
(I11N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARL5C
(R35Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARL5C
(S151L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ARL5C, CACNB1
+13 more
Copy number gain
not provided
GUncertain significance
AATF, ABHD15
+201 more
Copy number gain
not provided
GPathogenic
STARD3, CDK12
+22 more
Copy number gain
not provided
GUncertain significance
ARL5C, CACNB1
+12 more
Copy number gain
See cases
GUncertain significance
ALOX12, ALOX12B
+1143 more
Copy number gain
See cases
GPathogenic
SPEM2, TBCD
+1143 more
Copy number gain
See cases
GPathogenic
ARL5C, CACNB1
+50 more
Copy number gain
See cases
GLikely benign
AARSD1, AATF
+2032 more
Copy number gain
See cases
GPathogenic
LOC126862582, LOC126862583
+1753 more
Copy number gain
See cases
GPathogenic
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