"Ambry Genetics"[submitter] AND "GPAT4"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623425	NM_178819.4(GPAT4):c.127C>G (p.Arg43Gly)	GPAT4 (R43G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540849	NM_178819.4(GPAT4):c.182T>C (p.Met61Thr)	GPAT4, LOC126860367 (M61T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323616	NM_178819.4(GPAT4):c.188G>A (p.Arg63Gln)	GPAT4, LOC126860367 (R63Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246199	NM_178819.4(GPAT4):c.207C>A (p.Asn69Lys)	GPAT4, LOC126860367 (N69K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101135	NM_178819.4(GPAT4):c.278A>G (p.Lys93Arg)	GPAT4, LOC126860367 (K93R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383034	NM_178819.4(GPAT4):c.637G>A (p.Val213Ile)	GPAT4 (V5I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101136	NM_178819.4(GPAT4):c.688A>G (p.Thr230Ala)	GPAT4 (T230A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101137	NM_178819.4(GPAT4):c.839C>T (p.Ala280Val)	GPAT4 (A280V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596367	NM_178819.4(GPAT4):c.862G>A (p.Val288Ile)	GPAT4 (V288I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101138	NM_178819.4(GPAT4):c.878C>T (p.Ser293Leu)	GPAT4 (S85L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101132	NM_178819.4(GPAT4):c.1121G>A (p.Arg374Gln)	GPAT4 (R374Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397073	NM_178819.4(GPAT4):c.1172T>A (p.Met391Lys)	GPAT4 (M183K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101133	NM_178819.4(GPAT4):c.1267G>T (p.Gly423Trp)	GPAT4 (G423W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217835	NM_178819.4(GPAT4):c.1298C>T (p.Thr433Met)	GPAT4 (T225M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101134	NM_178819.4(GPAT4):c.1351A>G (p.Lys451Glu)	GPAT4 (K243E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign