"Ambry Genetics"[submitter] AND "AFP"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274910	NM_001134.3(AFP):c.118G>A (p.Glu40Lys)	AFP (E40K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274889	NM_001134.3(AFP):c.167A>G (p.Gln56Arg)	AFP (Q56R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471348	NM_001134.3(AFP):c.286G>A (p.Glu96Lys)	AFP (E96K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093344	NM_001134.3(AFP):c.394A>C (p.Thr132Pro)	AFP (T132P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597245	NM_001134.3(AFP):c.401C>T (p.Ala134Val)	AFP (A134V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595416	NM_001134.3(AFP):c.406A>T (p.Ile136Phe)	AFP (I136F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361426	NM_001134.3(AFP):c.418C>A (p.Gln140Lys)	AFP (Q140K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093354	NM_001134.3(AFP):c.428A>C (p.Glu143Ala)	AFP (E143A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358456	NM_001134.3(AFP):c.550C>T (p.Arg184Cys)	AFP (R184C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588408	NM_001134.3(AFP):c.712A>C (p.Ile238Leu)	AFP (I238L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527773	NM_001134.3(AFP):c.823C>G (p.Leu275Val)	AFP (L275V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319744	NM_001134.3(AFP):c.881C>T (p.Thr294Ile)	AFP (T136I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2289110	NM_001134.3(AFP):c.932G>A (p.Gly311Asp)	AFP (G153D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618742	NM_001134.3(AFP):c.941T>C (p.Ile314Thr)	AFP (I156T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479955	NM_001134.3(AFP):c.944T>C (p.Ile315Thr)	AFP (I315T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327412	NM_001134.3(AFP):c.962A>C (p.Glu321Ala)	AFP (E163A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274878	NM_001134.3(AFP):c.1001T>C (p.Leu334Ser)	AFP (L334S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538756	NM_001134.3(AFP):c.1045A>G (p.Ile349Val)	AFP (I191V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322297	NM_001134.3(AFP):c.1171C>G (p.Leu391Val)	AFP (L233V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274900	NM_001134.3(AFP):c.1178G>A (p.Cys393Tyr)	AFP (C235Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521111	NM_001134.3(AFP):c.1334C>T (p.Ser445Leu)	AFP, LOC126807077 (S445L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274914	NM_001134.3(AFP):c.1426G>A (p.Ala476Thr)	AFP, LOC126807077 (A476T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274642	NM_001134.3(AFP):c.1427C>T (p.Ala476Val)	AFP, LOC126807077 (A318V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258889	NM_001134.3(AFP):c.1439T>C (p.Ile480Thr)	AFP (I480T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233431	NM_001134.3(AFP):c.1466A>C (p.Glu489Ala)	AFP (E489A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411733	NM_001134.3(AFP):c.1594A>G (p.Ile532Val)	AFP (I532V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536021	NM_001134.3(AFP):c.1599C>G (p.Phe533Leu)	AFP (F375L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093318	NM_001134.3(AFP):c.1621C>A (p.Gln541Lys)	AFP (Q383K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093322	NM_001134.3(AFP):c.1674G>C (p.Lys558Asn)	AFP (K558N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093324	NM_001134.3(AFP):c.1693G>C (p.Glu565Gln)	AFP (E565Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093331	NM_001134.3(AFP):c.1767A>T (p.Glu589Asp)	AFP (E431D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382345	NM_001134.3(AFP):c.1816G>T (p.Ala606Ser)	AFP (A448S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32