U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPB7
(R159Q +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(R151W +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(P155L +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(R139H +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(R136W +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(T148A +7 more)
Single nucleotide variant
(missense variant)
Oromandibular-limb hypogenesis spectrum
GLikely benign
HSPB7
(R128P +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
Single nucleotide variant
(synonymous variant)
not provided
GBenign
HSPB7
(A118V +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(F127L +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(V112I +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(A103T +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(R112W +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(A160V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(G75E +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(D126G +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
HSPB7
(D126N +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
HSPB7
(D125A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(L120P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(P114L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSPB7
(L34P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HSPB7
(S29L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
Format
Items per page
Sort by
Choose Destination