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Links from Gene

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862572, TMEM101
(I15F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(G6R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(K4N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(L22P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(A24V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126862572, TMEM101
(G6S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(C26Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
(A34T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126862572, TMEM101
(I95N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126862572, TMEM101
(G30C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126862572, TMEM101
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
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