ERMN[gene] and "single gene"[properties] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2247678	NM_020711.3(ERMN):c.767C>A (p.Ser256Tyr)	ERMN (S269Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545318	NM_020711.3(ERMN):c.743G>A (p.Ser248Asn)	ERMN (S228N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511380	NM_020711.3(ERMN):c.611T>C (p.Ile204Thr)	ERMN (I217T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532970	NM_020711.3(ERMN):c.590A>G (p.Asp197Gly)	ERMN (D177G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090306	NM_020711.3(ERMN):c.577A>G (p.Asn193Asp)	ERMN (N173D +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2394103	NM_020711.3(ERMN):c.572A>G (p.Asp191Gly)	ERMN (D191G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347551	NM_020711.3(ERMN):c.563A>G (p.Asp188Gly)	ERMN (D168G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507869	NM_020711.3(ERMN):c.506A>T (p.Asp169Val)	ERMN (D182V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590415	NM_020711.3(ERMN):c.452G>A (p.Gly151Asp)	ERMN (G151D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512210	NM_020711.3(ERMN):c.439A>G (p.Arg147Gly)	ERMN (R127G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090305	NM_020711.3(ERMN):c.430G>T (p.Asp144Tyr)	ERMN (D157Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478920	NM_020711.3(ERMN):c.429A>C (p.Glu143Asp)	ERMN (E143D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382171	NM_020711.3(ERMN):c.428A>C (p.Glu143Ala)	ERMN (E143A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274727	NM_020711.3(ERMN):c.368G>T (p.Ser123Ile)	ERMN (S123I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243715	NM_020711.3(ERMN):c.355C>T (p.Pro119Ser)	ERMN (P119S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359334	NM_020711.3(ERMN):c.328A>G (p.Arg110Gly)	ERMN (R123G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233992	NM_020711.3(ERMN):c.247C>T (p.Pro83Ser)	ERMN (P83S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2338352	NM_020711.3(ERMN):c.202A>G (p.Met68Val)	ERMN (M68V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783123	NM_020711.3(ERMN):c.154G>A (p.Ala52Thr)	ERMN (A52T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2264974	NM_020711.3(ERMN):c.70C>G (p.Gln24Glu)	ERMN (Q37E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282978	NM_020711.3(ERMN):c.52C>T (p.Pro18Ser)	ERMN (P31S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471536	NM_020711.3(ERMN):c.32C>A (p.Ala11Asp)	ERMN (A24D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22