Related gene-specific medical variations for Gene (Select 114790) - ClinVar - NCBI

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Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323279	NM_052902.4(STK11IP):c.808C>T (p.Arg270Trp)	LOC126806519, STK11IP (R270W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323272	NM_052902.4(STK11IP):c.845G>A (p.Arg282His)	LOC126806519, STK11IP (R282H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171272	NM_052902.4(STK11IP):c.770G>A (p.Arg257Gln)	LOC126806519, STK11IP (R257Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171270	NM_052902.4(STK11IP):c.640C>A (p.Leu214Met)	LOC126806519, STK11IP (L214M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607974	NM_052902.4(STK11IP):c.719G>A (p.Arg240Gln)	LOC126806519, STK11IP (R240Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519017	NM_052902.4(STK11IP):c.868C>G (p.Pro290Ala)	LOC126806519, STK11IP (P290A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518967	NM_052902.4(STK11IP):c.668T>C (p.Leu223Ser)	LOC126806519, STK11IP (L223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475804	NM_052902.4(STK11IP):c.845G>T (p.Arg282Leu)	LOC126806519, STK11IP (R282L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462900	NM_052902.4(STK11IP):c.694G>T (p.Ala232Ser)	LOC126806519, STK11IP (A232S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381655	NM_052902.4(STK11IP):c.659G>A (p.Arg220His)	LOC126806519, STK11IP (R220H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2306100	NM_052902.4(STK11IP):c.751G>A (p.Glu251Lys)	LOC126806519, STK11IP (E251K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214175	NM_052902.4(STK11IP):c.658C>T (p.Arg220Cys)	LOC126806519, STK11IP (R220C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance