"PreventionGenetics, part of Exact Sciences"[submitter] AND "ATRN"[gen - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041871	NM_139321.3(ATRN):c.-44T>G	ATRN, LOC130065331	Single nucleotide variant (5 prime UTR variant)	ATRN-related disorder	GLikely benign
Select item 1664699	NM_139321.3(ATRN):c.63G>A (p.Ala21=)	ATRN, LOC130065331	Single nucleotide variant (synonymous variant +1 more)	ATRN-related disorder +1 more	GLikely benign
Select item 3047881	NM_139321.3(ATRN):c.177A>C (p.Pro59=)	ATRN, LOC130065331	Single nucleotide variant (synonymous variant +1 more)	ATRN-related disorder	GLikely benign
Select item 2631059	NM_139321.3(ATRN):c.379G>T (p.Glu127Ter)	ATRN (E127*)	Single nucleotide variant (nonsense +1 more)	ATRN-related disorder	GUncertain significance
Select item 3052390	NM_139321.3(ATRN):c.402C>T (p.Gly134=)	ATRN	Single nucleotide variant (synonymous variant +1 more)	ATRN-related disorder	GLikely benign
Select item 1170767	NM_139321.3(ATRN):c.435G>A (p.Val145=)	ATRN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1165619	NM_139321.3(ATRN):c.462C>T (p.Tyr154=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GBenign
Select item 3035309	NM_139321.3(ATRN):c.468G>A (p.Thr156=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder	GLikely benign
Select item 2629116	NM_139321.3(ATRN):c.491G>T (p.Gly164Val)	ATRN (G164V +1 more)	Single nucleotide variant (missense variant)	ATRN-related disorder +1 more	GUncertain significance
Select item 1638954	NM_139321.3(ATRN):c.615C>T (p.Leu205=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GLikely benign
Select item 2041371	NM_139321.3(ATRN):c.726T>C (p.Asn242=)	ATRN	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3053188	NM_139321.3(ATRN):c.798C>T (p.Ser266=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder	GLikely benign
Select item 2315399	NM_139321.3(ATRN):c.952T>C (p.Cys318Arg)	ATRN (C318R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2041372	NM_139321.3(ATRN):c.1159A>G (p.Asn387Asp)	ATRN (N271D +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3035251	NM_139321.3(ATRN):c.1203+8A>G	ATRN	Single nucleotide variant (intron variant)	ATRN-related disorder	GLikely benign
Select item 1167765	NM_139321.3(ATRN):c.1277T>C (p.Ile426Thr)	ATRN (I310T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 719120	NM_139321.3(ATRN):c.1357A>T (p.Thr453Ser)	ATRN (T337S +1 more)	Single nucleotide variant (missense variant)	ATRN-related disorder +1 more	GBenign
Select item 1594815	NM_139321.3(ATRN):c.1545C>T (p.Tyr515=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GLikely benign
Select item 1165620	NM_139321.3(ATRN):c.2892C>T (p.Tyr964=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GBenign
Select item 723716	NM_139321.3(ATRN):c.3417-3dup	ATRN	Duplication (intron variant)	ATRN-related disorder +1 more	GBenign
Select item 1167767	NM_139321.3(ATRN):c.3455G>A (p.Arg1152Lys)	ATRN (R1036K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 773086	NM_139321.3(ATRN):c.3676G>A (p.Val1226Ile)	ATRN (V1110I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1900554	NM_139321.3(ATRN):c.3909C>A (p.Ile1303=)	ATRN	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1165621	NM_139321.3(ATRN):c.4080G>A (p.Pro1360=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GBenign
Select item 1169881	NM_139321.3(ATRN):c.4098C>T (p.Ala1366=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder +1 more	GBenign
Select item 2065327	NM_139321.3(ATRN):c.4137G>A (p.Leu1379=)	ATRN	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3052923	NM_139321.3(ATRN):c.4278G>C (p.Gly1426=)	ATRN	Single nucleotide variant (synonymous variant)	ATRN-related disorder	GLikely benign

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Items: 27