U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRAS
(A130I)
Indel
(missense variant)
Cerebral arteriovenous malformation
+12 more
GUncertain significance
KRAS
(I187V)
Single nucleotide variant
(missense variant +1 more)
Autoimmune lymphoproliferative syndrome type 4
GUncertain significance
KRAS
Single nucleotide variant
(intron variant)
Acute myeloid leukemia
+12 more
GConflicting classifications of pathogenicity
KRAS
Deletion
(3 prime UTR variant +1 more)
Noonan syndrome
+13 more
GUncertain significance
KRAS
Single nucleotide variant
(intron variant)
not provided
+12 more
GBenign/Likely benign
NRAS
(V9I)
Single nucleotide variant
(missense variant)
Large congenital melanocytic nevus
+8 more
GUncertain significance
KRAS
Single nucleotide variant
(intron variant)
RASopathy
+13 more
GBenign/Likely benign
KRAS
(A146P)
Single nucleotide variant
(missense variant)
Autoimmune lymphoproliferative syndrome type 4
+1 more
GPathogenic/Likely pathogenic
KRAS
(A130V)
Single nucleotide variant
(missense variant)
not provided
+15 more
GUncertain significance
KRAS
Single nucleotide variant
(intron variant)
Familial cancer of breast
+12 more
GLikely benign
KRAS
Single nucleotide variant
(intron variant)
Familial cancer of breast
+12 more
GLikely benign
KRAS
Single nucleotide variant
(synonymous variant)
RASopathy
GLikely benign
KRAS
(G13C)
Single nucleotide variant
(missense variant)
Non-small cell lung carcinoma
+3 more
GPathogenic/Likely pathogenic
KRAS
Single nucleotide variant
(synonymous variant)
RASopathy
GLikely benign
KRAS
(D119N)
Single nucleotide variant
(missense variant)
Autoimmune lymphoproliferative syndrome type 4
+5 more
GLikely pathogenic
KRAS
(Q22R)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic
NRAS
(G12D)
Single nucleotide variant
(missense variant)
NRAS-related condition
+5 more
GPathogenic/Likely pathogenic
NRAS
(G13D)
Single nucleotide variant
(missense variant)
Acute megakaryoblastic leukemia in down syndrome
+2 more
GPathogenic/Likely pathogenic
KRAS
(P34R)
Single nucleotide variant
(missense variant)
Cardio-facio-cutaneous syndrome
+7 more
GPathogenic/Likely pathogenic
KRAS
(D153V)
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome
GPathogenic
KRAS
(G12D)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
KRAS
(G13D)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination