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Links from Gene

Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLYBL, CLYBL-AS3
(A300P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(A300T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(D320V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(W293C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(M230T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(R225Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL-AS3, CLYBL
(R174Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC112163637, CLYBL
(L18V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(A17V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(L94V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(D73Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(T185N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(A13V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(A17S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(R87Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(R4C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(R11G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(R45Q)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(A263T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(S215G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(R127Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(T298M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(A17T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(V189I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CLYBL, CLYBL-AS3
(I232T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(V167I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, LOC112163637
(A2G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(P136R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL, CLYBL-AS3
(D164H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CLYBL
Copy number loss
not provided
GLikely benign
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