"Ambry Genetics"[submitter] AND "CEACAM8"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3141853	NM_001816.4(CEACAM8):c.1034G>T (p.Arg345Met)	CEACAM8, LIPE-AS1 (R345M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141852	NM_001816.4(CEACAM8):c.1034G>A (p.Arg345Lys)	CEACAM8, LIPE-AS1 (R345K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247778	NM_001816.4(CEACAM8):c.1024G>A (p.Val342Ile)	CEACAM8, LIPE-AS1 (V342I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2523612	NM_001816.4(CEACAM8):c.945G>A (p.Met315Ile)	CEACAM8, LIPE-AS1 (M315I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141856	NM_001816.4(CEACAM8):c.878A>T (p.Asn293Ile)	CEACAM8, LIPE-AS1 (N293I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221083	NM_001816.4(CEACAM8):c.868A>G (p.Thr290Ala)	CEACAM8, LIPE-AS1 (T290A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326999	NM_001816.4(CEACAM8):c.782C>A (p.Ala261Glu)	CEACAM8, LIPE-AS1 (A261E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141855	NM_001816.4(CEACAM8):c.743A>G (p.Tyr248Cys)	CEACAM8, LIPE-AS1 (Y248C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493901	NM_001816.4(CEACAM8):c.742T>G (p.Tyr248Asp)	CEACAM8, LIPE-AS1 (Y248D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554943	NM_001816.4(CEACAM8):c.737A>T (p.Asp246Val)	CEACAM8, LIPE-AS1 (D246V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322693	NM_001816.4(CEACAM8):c.662C>T (p.Ala221Val)	CEACAM8, LIPE-AS1 (A221V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2377417	NM_001816.4(CEACAM8):c.659C>G (p.Pro220Arg)	CEACAM8, LIPE-AS1 (P220R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2528566	NM_001816.4(CEACAM8):c.640G>A (p.Glu214Lys)	CEACAM8, LIPE-AS1 (E214K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350536	NM_001816.4(CEACAM8):c.632G>A (p.Gly211Glu)	CEACAM8, LIPE-AS1 (G211E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342059	NM_001816.4(CEACAM8):c.557C>T (p.Pro186Leu)	CEACAM8, LIPE-AS1 (P186L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558740	NM_001816.4(CEACAM8):c.548A>T (p.Gln183Leu)	CEACAM8, LIPE-AS1 (Q183L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544530	NM_001816.4(CEACAM8):c.508G>C (p.Glu170Gln)	CEACAM8, LIPE-AS1 (E170Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237254	NM_001816.4(CEACAM8):c.425C>T (p.Pro142Leu)	CEACAM8, LIPE-AS1 (P142L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141854	NM_001816.4(CEACAM8):c.293G>A (p.Arg98Gln)	CEACAM8, LIPE-AS1 (R98Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589249	NM_001816.4(CEACAM8):c.233G>A (p.Arg78Gln)	CEACAM8, LIPE-AS1 (R78Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259109	NM_001816.4(CEACAM8):c.232C>G (p.Arg78Gly)	CEACAM8, LIPE-AS1 (R78G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457488	NM_001816.4(CEACAM8):c.226A>C (p.Asn76His)	CEACAM8, LIPE-AS1 (N76H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371065	NM_001816.4(CEACAM8):c.215C>G (p.Thr72Arg)	CEACAM8, LIPE-AS1 (T72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211656	NM_001816.4(CEACAM8):c.211G>A (p.Glu71Lys)	CEACAM8, LIPE-AS1 (E71K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225074	NM_001816.4(CEACAM8):c.188G>A (p.Arg63His)	CEACAM8, LIPE-AS1 (R63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467161	NM_001816.4(CEACAM8):c.141G>C (p.Glu47Asp)	CEACAM8, LIPE-AS1 (E47D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26