"Ambry Genetics"[submitter] AND "TMEM86B"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2269943	NM_173804.5(TMEM86B):c.661C>T (p.Pro221Ser)	TMEM86B (P221S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463639	NM_173804.5(TMEM86B):c.622G>A (p.Ala208Thr)	TMEM86B (A207T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333133	NM_173804.5(TMEM86B):c.611C>A (p.Thr204Asn)	TMEM86B (T203N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512020	NM_173804.5(TMEM86B):c.595C>T (p.His199Tyr)	TMEM86B (H198Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618160	NM_173804.5(TMEM86B):c.578A>G (p.Gln193Arg)	TMEM86B (Q192R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179678	NM_173804.5(TMEM86B):c.553G>A (p.Val185Met)	TMEM86B (V185M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296232	NM_173804.5(TMEM86B):c.520T>C (p.Trp174Arg)	TMEM86B (W173R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466526	NM_173804.5(TMEM86B):c.508G>A (p.Gly170Arg)	TMEM86B (G170R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393751	NM_173804.5(TMEM86B):c.508G>C (p.Gly170Arg)	TMEM86B (G169R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352111	NM_173804.5(TMEM86B):c.493G>A (p.Gly165Ser)	TMEM86B (G164S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179676	NM_173804.5(TMEM86B):c.491G>A (p.Arg164His)	TMEM86B (R163H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489250	NM_173804.5(TMEM86B):c.479C>T (p.Ala160Val)	TMEM86B (A160V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247149	NM_173804.5(TMEM86B):c.451G>A (p.Val151Met)	TMEM86B (V151M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179675	NM_173804.5(TMEM86B):c.449C>G (p.Pro150Arg)	TMEM86B (P150R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371832	NM_173804.5(TMEM86B):c.449C>T (p.Pro150Leu)	TMEM86B (P149L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407921	NM_173804.5(TMEM86B):c.319G>A (p.Ala107Thr)	TMEM86B (A107T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2380271	NM_173804.5(TMEM86B):c.253G>C (p.Ala85Pro)	PPP6R1, TMEM86B (A85P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179673	NM_173804.5(TMEM86B):c.212G>A (p.Gly71Glu)	PPP6R1, TMEM86B (G70E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286138	NM_173804.5(TMEM86B):c.211G>A (p.Gly71Arg)	PPP6R1, TMEM86B (G70R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257883	NM_173804.5(TMEM86B):c.122C>G (p.Pro41Arg)	PPP6R1, TMEM86B (P40R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457953	NM_173804.5(TMEM86B):c.100G>A (p.Val34Met)	PPP6R1, TMEM86B (V33M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21