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Links from Gene

Items: 49

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRRC7, LRRC7-AS1
(G1016* +3 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(G1009E +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
LRRC7
(R600P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRC7
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(P1131fs +3 more)
Insertion
(frameshift variant)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(P1202L +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(L920fs +3 more)
Duplication
(non-coding transcript variant +1 more)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(N795D +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(R741Q +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(V1098A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(T1212R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(G1136R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(R1130G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(Q1069K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(A1105T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(G1049E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(M1007V +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P969A +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S831P +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(Q864K +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S952T +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(H1017Q +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S1015R +3 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P1120L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(A1093V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S667C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(W1255G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(Y1049C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(Y1048H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P1085L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7
(E26Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRC7, LRRC7-AS1
(E964K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(A1089T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S757L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(D1020G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(A750S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P753L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S972fs +3 more)
Deletion
(frameshift variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(R845C +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P901T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P875S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S1126N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(S789L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(D808G +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P778L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(P1131S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LRRC7, LRRC7-AS1
(Y1177* +3 more)
Single nucleotide variant
(nonsense)
Intellectual disability
GUncertain significance
LRRC7
Copy number gain
See cases
GLikely benign
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