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Links from Gene

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCDC2B, TMEM234
(S283T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126805686, TMEM234
(V116G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126805687, TMEM234
(Q7R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DCDC2B, TMEM234
(A291T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126805687, TMEM234
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC126805687, TMEM234
(T55I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DCDC2B, TMEM234
(Y289H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126805687, TMEM234
(S4T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DCDC2B, TMEM234
(A239S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126805687, TMEM234
(Q43P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126805687, TMEM234
(T50I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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