Related gene-specific medical variations for Gene (Select 9479) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3123311	NM_005456.4(MAPK8IP1):c.88C>T (p.Pro30Ser)	LOC130005631, MAPK8IP1 (P30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3051609	NM_005456.4(MAPK8IP1):c.-5C>T	LOC130005631, MAPK8IP1	Single nucleotide variant (5 prime UTR variant)	MAPK8IP1-related condition	GLikely benign
Select item 2665083	NM_005456.4(MAPK8IP1):c.1666+5T>C	MAPK8IP1	Single nucleotide variant (intron variant)	Type 2 diabetes mellitus	GUncertain significance
Select item 2546079	NM_005456.4(MAPK8IP1):c.52G>C (p.Ala18Pro)	LOC130005631, MAPK8IP1 (A18P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538701	NM_005456.4(MAPK8IP1):c.19G>C (p.Gly7Arg)	LOC130005631, MAPK8IP1 (G7R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312544	NM_005456.4(MAPK8IP1):c.82G>C (p.Ala28Pro)	LOC130005631, MAPK8IP1 (A28P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291784	NM_005456.4(MAPK8IP1):c.209C>T (p.Pro70Leu)	LOC112081396, MAPK8IP1 (P70L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224628	NM_005456.4(MAPK8IP1):c.32G>C (p.Gly11Ala)	LOC130005631, MAPK8IP1 (G11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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