"Ambry Genetics"[submitter] AND "ICAM4-AS1"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2461507	NM_001544.5(ICAM4):c.52C>T (p.Pro18Ser)	ICAM4, ICAM4-AS1 (P18S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619181	NM_001544.5(ICAM4):c.127G>A (p.Gly43Arg)	ICAM4, ICAM4-AS1 (G43R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2620460	NM_001544.5(ICAM4):c.145T>C (p.Trp49Arg)	ICAM4, ICAM4-AS1 (W49R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2406780	NM_001544.5(ICAM4):c.159C>A (p.Ser53Arg)	ICAM4, ICAM4-AS1 (S53R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352983	NM_001544.5(ICAM4):c.182C>T (p.Pro61Leu)	ICAM4, ICAM4-AS1 (P61L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321610	NM_001544.5(ICAM4):c.374C>T (p.Thr125Ile)	ICAM4, ICAM4-AS1 (T125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542781	NM_001544.5(ICAM4):c.422C>T (p.Pro141Leu)	ICAM4, ICAM4-AS1 (P141L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107913	NM_001544.5(ICAM4):c.464T>C (p.Val155Ala)	ICAM4, ICAM4-AS1 (V155A)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2276367	NM_001544.5(ICAM4):c.479C>G (p.Pro160Arg)	ICAM4, ICAM4-AS1 (P160R)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3107915	NM_001544.5(ICAM4):c.490T>A (p.Leu164Met)	ICAM4, ICAM4-AS1 (L138H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2467837	NM_001544.5(ICAM4):c.508C>T (p.His170Tyr)	ICAM4, ICAM4-AS1 (A144V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107916	NM_001544.5(ICAM4):c.544C>T (p.Arg182Cys)	ICAM4, ICAM4-AS1 (A156V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2279696	NM_001544.5(ICAM4):c.586G>A (p.Glu196Lys)	ICAM4, ICAM4-AS1 (E196K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483233	NM_001544.5(ICAM4):c.616C>A (p.Gln206Lys)	ICAM4, ICAM4-AS1 (A180E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107917	NM_001544.5(ICAM4):c.648C>T (p.Leu216=)	ICAM4, ICAM4-AS1 (R191*)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 2304593	NM_001544.5(ICAM4):c.674C>G (p.Ser225Trp)	ICAM4, ICAM4-AS1 (S225W)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3107918	NM_001544.5(ICAM4):c.678A>C (p.Ala226=)	ICAM4, ICAM4-AS1 (T201P)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 2325905	NM_001544.5(ICAM4):c.691A>G (p.Met231Val)	ICAM4, ICAM4-AS1 (M231V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597454	NM_001544.5(ICAM4):c.709G>A (p.Ala237Thr)	ICAM4, ICAM4-AS1 (A237T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance