C1864839[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 330620	NM_003597.5(KLF11):c.-31G>A	KLF11, LOC128897170	Single nucleotide variant (5 prime UTR variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 1635997	NM_003597.5(KLF11):c.42+18C>G	KLF11	Single nucleotide variant (intron variant)	Maturity-onset diabetes of the young type 7 +1 more	GLikely benign
Select item 330622	NM_003597.5(KLF11):c.86G>A (p.Arg29Gln)	KLF11 (R29Q +1 more)	Single nucleotide variant (missense variant)	Monogenic diabetes +2 more	GBenign/Likely benign
Select item 1316948	NM_003597.5(KLF11):c.225C>T (p.Val75=)	KLF11	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 330623	NM_003597.5(KLF11):c.259A>G (p.Met87Val)	KLF11 (M87V +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 330626	NM_003597.5(KLF11):c.358A>G (p.Arg120Gly)	KLF11 (R120G +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 330627	NM_003597.5(KLF11):c.429C>T (p.Ala143=)	KLF11	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 892905	NM_003597.5(KLF11):c.431T>C (p.Val144Ala)	KLF11 (V127A +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 1430360	NM_003597.5(KLF11):c.437C>T (p.Ala146Val)	KLF11 (A146V +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 393366	NM_003597.5(KLF11):c.541G>A (p.Glu181Lys)	KLF11 (E181K +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GLikely benign
Select item 892908	NM_003597.5(KLF11):c.608G>A (p.Gly203Glu)	KLF11 (G203E +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +1 more	GUncertain significance
Select item 893715	NM_003597.5(KLF11):c.673A>C (p.Ser225Arg)	KLF11 (S225R +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +2 more	GUncertain significance
Select item 1337221	NM_003597.5(KLF11):c.811A>C (p.Lys271Gln)	KLF11 (K254Q +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 893716	NM_003597.5(KLF11):c.870C>T (p.Ile290=)	KLF11	Single nucleotide variant (synonymous variant)	Maturity-onset diabetes of the young type 7	GLikely benign
Select item 893981	NM_003597.5(KLF11):c.961G>C (p.Ala321Pro)	KLF11 (A321P +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 1431303	NM_003597.5(KLF11):c.992G>T (p.Gly331Val)	KLF11 (G331V +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +1 more	GUncertain significance
Select item 1497699	NM_003597.5(KLF11):c.1037G>T (p.Gly346Val)	KLF11 (G329V +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +1 more	GUncertain significance
Select item 893982	NM_003597.5(KLF11):c.1049C>T (p.Pro350Leu)	KLF11 (P333L +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 1645173	NM_003597.5(KLF11):c.1050G>A (p.Pro350=)	KLF11	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 330639	NM_003597.5(KLF11):c.1169G>A (p.Arg390Gln)	KLF11 (R390Q +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7	GUncertain significance
Select item 1336833	NM_003597.5(KLF11):c.1396A>T (p.Ser466Cys)	KLF11 (S449C +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 892940	NM_003597.5(KLF11):c.1486G>A (p.Ala496Thr)	KLF11 (A496T +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +1 more	GConflicting classifications of pathogenicity
Select item 892941	NM_003597.5(KLF11):c.1503G>A (p.Pro501=)	KLF11	Single nucleotide variant (synonymous variant)	Maturity-onset diabetes of the young type 7 +1 more	GLikely benign

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Items: 23