Related gene-specific medical variations for Gene (Select 2633) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280927	NM_002053.3(GBP1):c.907G>A (p.Ala303Thr)	GBP1, LOC126805784 (A303T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098882	NM_002053.3(GBP1):c.991G>T (p.Ala331Ser)	GBP1, LOC126805784 (A331S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098881	NM_002053.3(GBP1):c.887T>C (p.Leu296Pro)	GBP1, LOC126805784 (L296P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098875	NM_002053.3(GBP1):c.1175G>A (p.Arg392Gln)	GBP1, LOC126805784 (R392Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519514	NM_002053.3(GBP1):c.1009C>G (p.Gln337Glu)	GBP1, LOC126805784 (Q337E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511570	NM_002053.3(GBP1):c.1073G>C (p.Arg358Thr)	GBP1, LOC126805784 (R358T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489128	NM_002053.3(GBP1):c.1154C>T (p.Ala385Val)	GBP1, LOC126805784 (A385V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456965	NM_002053.3(GBP1):c.1167A>C (p.Glu389Asp)	GBP1, LOC126805784 (E389D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2455384	NM_002053.3(GBP1):c.1172A>G (p.Lys391Arg)	GBP1, LOC126805784 (K391R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268897	NM_002053.3(GBP1):c.908C>T (p.Ala303Val)	GBP1, LOC126805784 (A303V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263433	NM_002053.3(GBP1):c.1229T>C (p.Leu410Ser)	GBP1, LOC126805784 (L410S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance