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Links from Gene

Items: 1 to 100 of 145

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STARD13
(N342D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(V832D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(V678I +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
STARD13
(P506S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(T812M +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(A45V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(H1007Y +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(E979K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R856H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P712L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(D677H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(E730Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(L476P +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R410W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(V320A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R36C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CDX2, AMER2
+82 more
Copy number gain
not provided
GUncertain significance
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
STARD13
(P512L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P991H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(L955V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(F408S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(S295N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R874K +4 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
STARD13
(M290T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(Q1005H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(I1037T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P217L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(N441D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(I517V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(A1084T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(S301L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(A717V +4 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
STARD13
(Q24R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(R725Q +4 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
STARD13
(D99N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(S367R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P636S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(S507A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(Q1018R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R254C +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R581C +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(R427W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(M800T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(M26T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(T146M +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R588C +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(M529T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R569Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P185L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(H323N +4 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
STARD13
(R479W +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(S173C +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P1006L +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(A433T +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(L601F +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(M19T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(A886V +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(L497P +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(T510I +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R586Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(A351S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(K241R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(H245R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P563R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(T180M +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(P792S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(G544A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(D996A +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(T507M +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(L16Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(E121D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(E166G +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(D142Y +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(W469R +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(H48N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STARD13
(R241H +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STARD13
(R537Q +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
B3GLCT, BRCA2
+12 more
Copy number gain
not provided
Gnot provided
KL, RFC3
+1 more
Copy number gain
not provided
GUncertain significance
B3GLCT, HS6ST3
+332 more
Copy number gain
not provided
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
Complete trisomy 13 syndrome
GPathogenic
AKAP11, ALG11
+127 more
Copy number loss
not specified
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
not specified
GPathogenic
VPS36, VWA8
+329 more
Copy number gain
not specified
GPathogenic
ABCC4, ABHD13
+332 more
Copy number gain
not provided
GPathogenic
RFC3, STARD13
Copy number gain
not provided
GUncertain significance
DACH1, IRS2
+332 more
Copy number gain
See cases
GPathogenic
ALOX5AP, B3GLCT
+22 more
Copy number loss
not provided
GPathogenic
CENPJ, CHAMP1
+332 more
Copy number gain
See cases
GPathogenic
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign/Likely benign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign
STARD13
(P1000S +3 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GBenign
STARD13
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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