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

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109737	NM_006774.5(INMT):c.7G>A (p.Gly3Ser)	INMT, INMT-MINDY4 (G3S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2337804	NM_006774.5(INMT):c.98C>A (p.Pro33His)	INMT, INMT-MINDY4 (P33H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2351365	NM_006774.5(INMT):c.106G>A (p.Glu36Lys)	INMT, INMT-MINDY4 (E36K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3109732	NM_006774.5(INMT):c.127G>A (p.Glu43Lys)	INMT, INMT-MINDY4 (E43K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3286037	NM_006774.5(INMT):c.143C>T (p.Thr48Ile)	INMT, INMT-MINDY4 (T48I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2557535	NM_006774.5(INMT):c.230C>T (p.Ser77Phe)	INMT, INMT-MINDY4 (S76F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2368477	NM_006774.5(INMT):c.262G>A (p.Asp88Asn)	INMT, INMT-MINDY4 (D87N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2611167	NM_006774.5(INMT):c.274G>A (p.Glu92Lys)	INMT, INMT-MINDY4 (E91K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2616120	NM_006774.5(INMT):c.304C>A (p.Pro102Thr)	INMT, INMT-MINDY4 (P101T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2407343	NM_006774.5(INMT):c.363C>A (p.Ser121Arg)	INMT, INMT-MINDY4 (S120R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376078	NM_006774.5(INMT):c.370T>C (p.Trp124Arg)	INMT, INMT-MINDY4 (W123R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323025	NM_006774.5(INMT):c.400G>A (p.Ala134Thr)	INMT, INMT-MINDY4 (A133T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2522456	NM_006774.5(INMT):c.409C>T (p.Arg137Trp)	INMT, INMT-MINDY4 (R137W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109733	NM_006774.5(INMT):c.421T>C (p.Cys141Arg)	INMT, INMT-MINDY4 (C140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109734	NM_006774.5(INMT):c.502T>C (p.Cys168Arg)	INMT, INMT-MINDY4 (C167R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460640	NM_006774.5(INMT):c.530G>A (p.Arg177His)	INMT, INMT-MINDY4 (R176H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109735	NM_006774.5(INMT):c.572G>A (p.Gly191Asp)	INMT, INMT-MINDY4 (G191D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109736	NM_006774.5(INMT):c.598C>T (p.Arg200Trp)	INMT, INMT-MINDY4 (R199W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357285	NM_006774.5(INMT):c.605C>T (p.Pro202Leu)	INMT, INMT-MINDY4 (P201L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268799	NM_006774.5(INMT):c.624G>C (p.Lys208Asn)	INMT, INMT-MINDY4 (K207N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322348	NM_006774.5(INMT):c.657G>T (p.Glu219Asp)	INMT, INMT-MINDY4 (E219D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311692	NM_006774.5(INMT):c.720G>C (p.Gln240His)	INMT, INMT-MINDY4 (Q239H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286036	NM_006774.5(INMT):c.746A>G (p.Asn249Ser)	INMT, INMT-MINDY4 (N248S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2596286	NM_006774.5(INMT):c.772C>G (p.Arg258Gly)	INMT, INMT-MINDY4 (R257G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377716	NM_006774.5(INMT):c.773G>T (p.Arg258Leu)	INMT, INMT-MINDY4 (R257L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25