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Links from Gene

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRTAP9-1
(T70P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(P84T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLC4A1, DCAKD
+422 more
Copy number loss
Breast-ovarian cancer, familial, susceptibility to, 1
GPathogenic
KRTAP9-1
(P26T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(L212V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(C67W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(P40S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KRTAP9-1
(S33R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(C176Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(C62G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(P45A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(R216C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(C115Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(Q107H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(R231L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP9-1
(P232L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRT23, KRT39
+33 more
Copy number loss
not provided
GLikely benign
ALOX12, ALOX12B
+1143 more
Copy number gain
See cases
GPathogenic
SPEM2, TBCD
+1143 more
Copy number gain
See cases
GPathogenic
KRT23, KRT39
+36 more
Copy number loss
See cases
GLikely benign
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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