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Links from Gene

Items: 50

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT37
(P18L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(A36V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(S364R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R123H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(L373S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(L330P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC4A1, DCAKD
+422 more
Copy number loss
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
KRT37
(E260Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(L253V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R197C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(L175P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(V147A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(S441F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(A395T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R354H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R258Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(Q211P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(K232R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(Q211R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(I366L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(K121N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(I28T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(E144K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(S431I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R377W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(E128D)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
KRT37
(V393M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(D150N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R123C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(S145F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(G96S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(A222D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(T72I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(M43T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R396Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(E281K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(I302V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(A351G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(R354C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(A351T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37, LOC125177474
(I401F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(M43I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(G437R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(N48S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT37
(T7I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALOX12, ALOX12B
+1143 more
Copy number gain
See cases
GPathogenic
SPEM2, TBCD
+1143 more
Copy number gain
See cases
GPathogenic
AARSD1, AATF
+2032 more
Copy number gain
See cases
GPathogenic
LOC130060786, LOC130060787
+633 more
Copy number gain
See cases
GPathogenic
LOC126862582, LOC126862583
+1753 more
Copy number gain
See cases
GPathogenic
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