Related gene-specific medical variations for Gene (Select 4988) - ClinVar

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Links from Gene

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3286296	NM_001130700.2(IPCEF1):c.1080C>G (p.Ile360Met)	IPCEF1, OPRM1 (I359M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286295	NM_001130700.2(IPCEF1):c.783C>A (p.Asn261Lys)	IPCEF1, OPRM1 (N260K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286294	NM_001130700.2(IPCEF1):c.610A>G (p.Thr204Ala)	IPCEF1, OPRM1 (T203A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286292	NM_001130700.2(IPCEF1):c.508C>G (p.Pro170Ala)	IPCEF1, OPRM1 (P170A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286291	NM_001130700.2(IPCEF1):c.719C>T (p.Thr240Met)	IPCEF1, OPRM1 (T239M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286290	NM_001130700.2(IPCEF1):c.509C>T (p.Pro170Leu)	IPCEF1, OPRM1 (P169L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286289	NM_001130700.2(IPCEF1):c.517G>A (p.Ala173Thr)	IPCEF1, OPRM1 (A172T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461541	NM_001130700.2(IPCEF1):c.413C>T (p.Ser138Leu)	IPCEF1, OPRM1 (S137L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2406316	NM_001130700.2(IPCEF1):c.436A>T (p.Thr146Ser)	IPCEF1, OPRM1 (T145S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397512	NM_001130700.2(IPCEF1):c.421A>C (p.Ile141Leu)	IPCEF1, OPRM1 (I141L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364195	NM_001130700.2(IPCEF1):c.1312A>G (p.Ile438Val)	IPCEF1, OPRM1 (I438V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304027	NM_001130700.2(IPCEF1):c.923T>G (p.Val308Gly)	IPCEF1, OPRM1 (V308G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1277133	NM_001008503.3(OPRM1):c.1164+74814C>T	IPCEF1, OPRM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 829071	NM_001008503.3(OPRM1):c.1165-161T>G	IPCEF1, OPRM1	Single nucleotide variant (intron variant)	Tramadol response	Gdrug response
Select item 829070	NM_001008503.3(OPRM1):c.1165-151G>A	IPCEF1, OPRM1	Single nucleotide variant (intron variant)	Tramadol response	Gdrug response
Select item 829069	NM_001008503.3(OPRM1):c.1165-147C>T	IPCEF1, OPRM1	Single nucleotide variant (intron variant)	Tramadol response	Gdrug response
Select item 829068	NM_001008503.3(OPRM1):c.1165-1G>A	IPCEF1, OPRM1	Single nucleotide variant (synonymous variant +1 more)	Tramadol response	Gdrug response
Select item 829067	NM_001008503.3(OPRM1):c.1201C>T (p.Arg401Ter)	IPCEF1, OPRM1 (R401*)	Single nucleotide variant (synonymous variant +1 more)	Tramadol response	Gdrug response
Select item 829066	NM_001008503.3(OPRM1):c.*13C>T	IPCEF1, OPRM1	Single nucleotide variant (3 prime UTR variant +1 more)	Tramadol response	Gdrug response
Select item 829065	NM_001008503.3(OPRM1):c.*38C>T	IPCEF1, OPRM1	Single nucleotide variant (3 prime UTR variant +1 more)	Tramadol response	Gdrug response
Select item 829064	NM_001008503.3(OPRM1):c.*39C>T	IPCEF1, OPRM1	Single nucleotide variant (3 prime UTR variant +1 more)	Tramadol response	Gdrug response
Select item 829063	NM_001008503.3(OPRM1):c.*48G>T	IPCEF1, OPRM1	Single nucleotide variant (3 prime UTR variant +1 more)	Tramadol response	Gdrug response
Select item 828263	NM_001008503.3(OPRM1):c.1165-182T>C	IPCEF1, OPRM1	Single nucleotide variant (intron variant)	Tramadol response	Gdrug response
Select item 720651	NM_001130700.2(IPCEF1):c.553T>C (p.Ser185Pro)	IPCEF1, OPRM1 (S184P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 688857	GRCh37/hg19 6q25.2(chr6:154369847-154429434)x1	OPRM1	Copy number loss	not provided	GUncertain significance
Select item 157032	NM_001145279.3(OPRM1):c.-8245_-1+9405del	OPRM1	Deletion	Gestational diabetes mellitus uncontrolled	Gnot provided

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Links from Gene

Items: 26