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Items: 49

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(Y8C)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not provided
+5 more
GBenign/Likely benign
MSH6
(A36V)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 5
+8 more
GConflicting classifications of pathogenicity
MSH6
(G46R)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not specified
+4 more
GBenign/Likely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not provided
+4 more
GLikely benign
MSH6
(N112S)
Single nucleotide variant
(missense variant +2 more)
not specified
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(intron variant)
Lynch syndrome
GLikely benign
MSH6
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MSH6
(E220D +1 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GLikely benign
MSH6
(D132G +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH6
(E272D +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(T333I +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
MSH6
(V352I +2 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MSH6
(L396V +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH6
(R495* +2 more)
Single nucleotide variant
(nonsense)
Lynch syndrome
GPathogenic
MSH6
(S201C +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome
+2 more
GLikely benign
MSH6
(V509A +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GLikely benign
MSH6
(I622L +2 more)
Single nucleotide variant
(missense variant)
Endometrial carcinoma
+3 more
GUncertain significance
MSH6
(K632E +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
+5 more
GConflicting classifications of pathogenicity
MSH6
(T331S +8 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
(D649G +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MSH6
(P673L +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
MSH6
(I795T +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome 1
+6 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
MSH6
(K854M +2 more)
Single nucleotide variant
(missense variant)
MSH6-related disorder
+8 more
GConflicting classifications of pathogenicity
MSH6
(K854N +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MSH6
(I872K +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(V878A +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH6
(Q889H +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
MSH6
(R1024W +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH6
(I1054F +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
(R1076H +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+4 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome 1
GBenign
MSH6
(P1087S +2 more)
Single nucleotide variant
(missense variant)
MSH6-related disorder
+8 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
(V1173M +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
MSH6
Single nucleotide variant
(intron variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MSH6
(T1243S +2 more)
Single nucleotide variant
(missense variant)
not specified
+6 more
GConflicting classifications of pathogenicity
MSH6
(R1304K +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
(K1325del +2 more)
Microsatellite
(inframe_deletion)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GUncertain significance
MSH6
(N1327H +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
MSH6
Microsatellite
(splice donor variant)
Endometrial carcinoma
+8 more
GBenign/Likely benign
MSH6
Microsatellite
(splice donor variant)
Lynch syndrome
GLikely benign
MSH6
Duplication
(intron variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
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