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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MLH1
(N38H)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
MLH1
Single nucleotide variant
(intron variant)
Lynch syndrome
GPathogenic
MLH1
(S131* +2 more)
Single nucleotide variant
(nonsense +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GPathogenic
MLH1
Single nucleotide variant
(splice acceptor variant +1 more)
Lynch syndrome
GPathogenic
MLH1
Single nucleotide variant
(intron variant)
Lynch syndrome
GPathogenic
MLH1
Single nucleotide variant
(splice acceptor variant)
Lynch syndrome
GPathogenic
MLH1
(G244D +3 more)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GPathogenic
MLH1
(R265C +3 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
MLH1
Deletion
(splice acceptor variant +2 more)
Lynch syndrome
GPathogenic
MLH1
(K461* +5 more)
Single nucleotide variant
(nonsense)
Lynch syndrome
GPathogenic
MLH1
(R399fs +5 more)
Duplication
(frameshift variant)
Lynch syndrome
GPathogenic
MLH1
Single nucleotide variant
(splice donor variant)
Lynch syndrome
GPathogenic
MLH1
Indel
(splice donor variant)
Lynch syndrome
GPathogenic
MLH1
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GPathogenic
MLH1
Deletion
(splice acceptor variant +2 more)
Colorectal cancer, hereditary nonpolyposis, type 2
GPathogenic
MLH1
(M346fs +5 more)
Duplication
(frameshift variant +1 more)
Lynch syndrome
GPathogenic
MLH1
(I270fs +5 more)
Deletion
(frameshift variant +1 more)
Lynch syndrome
GPathogenic
MLH1
(L622H +5 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
MLH1
(M341fs +7 more)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
MLH1
(W714* +8 more)
Single nucleotide variant
(nonsense)
Hereditary nonpolyposis colorectal neoplasms
+4 more
GPathogenic
MLH1
(H678fs +8 more)
Duplication
(frameshift variant)
Lynch syndrome
GPathogenic
MLH1
(K410fs +7 more)
Deletion
(frameshift variant)
Lynch syndrome 1
GPathogenic
MLH1
Duplication
(frameshift variant +1 more)
Lynch syndrome
GPathogenic
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