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Links from Gene

Items: 25

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
H3C8
(V102A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(T81A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(K65R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(A112P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(S29R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(A128G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(A16T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(L101W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
H3C8
(V72M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
BTN2A1, BTN2A2
+42 more
Copy number gain
not specified
GUncertain significance
H3C8
(V36G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
H2BC7, H2BC8
+34 more
Copy number gain
not provided
GUncertain significance
TRX-CAT1-2, BTN3A1
+9 more
Copy number gain
not provided
GUncertain significance
H2BC10, H2BC9
+7 more
Copy number loss
not provided
GLikely benign
H1-3, H1-4
+24 more
Copy number gain
not provided
GUncertain significance
H1-1, H1-2
+33 more
Copy number gain
not provided
GUncertain significance
H1-1, H1-2
+34 more
Copy number gain
not provided
GUncertain significance
H2BC6, H3C4
+26 more
Copy number gain
not provided
GUncertain significance
H1-1, H1-2
+36 more
Copy number gain
not provided
GUncertain significance
AARS2, ABCC10
+1028 more
Copy number gain
See cases
GPathogenic
RING1, RIOK1
+1028 more
Copy number gain
See cases
GPathogenic
H3C4, H3C6
+24 more
Copy number gain
Breast ductal adenocarcinoma
GUncertain significance
ILRUN-AS1, IP6K3
+2582 more
Copy number gain
See cases
GPathogenic
H1-1, H1-2
+85 more
Copy number gain
See cases
GLikely benign
ABCF1, ABT1
+1340 more
Copy number gain
See cases
GPathogenic
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