"PreventionGenetics, part of Exact Sciences"[submitter] AND "TARS1"[ge - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782449	NM_152295.5(TARS1):c.62G>A (p.Gly21Asp)	TARS1 (G21D)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 3045118	NM_152295.5(TARS1):c.197C>T (p.Ala66Val)	TARS1 (A54V +1 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder	GLikely benign
Select item 771370	NM_152295.5(TARS1):c.231A>C (p.Glu77Asp)	TARS1 (E77D)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder +1 more	GBenign
Select item 2655386	NM_152295.5(TARS1):c.284C>A (p.Ala95Glu)	TARS1 (A83E +1 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder +1 more	GBenign
Select item 3041502	NM_152295.5(TARS1):c.330-954C>T	TARS1	Single nucleotide variant (intron variant)	TARS1-related disorder	GBenign
Select item 3037640	NM_152295.5(TARS1):c.330-4dup	TARS1	Duplication (intron variant)	TARS1-related disorder	GLikely benign
Select item 3060916	NM_152295.5(TARS1):c.330-4del	TARS1	Deletion (intron variant)	TARS1-related disorder	GLikely benign
Select item 3059544	NM_152295.5(TARS1):c.330-6_330-4del	TARS1	Deletion (intron variant)	TARS1-related disorder	GLikely benign
Select item 3055549	NM_152295.5(TARS1):c.330-5_330-4del	TARS1	Deletion (intron variant)	TARS1-related disorder	GLikely benign
Select item 3037841	NM_152295.5(TARS1):c.330-7_330-4del	TARS1	Deletion (intron variant)	TARS1-related disorder	GLikely benign
Select item 716827	NM_152295.5(TARS1):c.352G>A (p.Val118Ile)	TARS1 (V151I +1 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder +1 more	GBenign
Select item 771371	NM_152295.5(TARS1):c.525C>T (p.Tyr175=)	TARS1	Single nucleotide variant (synonymous variant +1 more)	TARS1-related disorder +1 more	GBenign
Select item 3056225	NM_152295.5(TARS1):c.693+6T>C	TARS1	Single nucleotide variant (intron variant)	TARS1-related disorder	GBenign
Select item 3033579	NM_152295.5(TARS1):c.977T>C (p.Ile326Thr)	TARS1 (I314T +2 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder	GLikely benign
Select item 3040429	NM_152295.5(TARS1):c.1155C>A (p.Thr385=)	TARS1	Single nucleotide variant (synonymous variant +1 more)	TARS1-related disorder	GBenign
Select item 3055451	NM_152295.5(TARS1):c.1506G>A (p.Pro502=)	LOC126807348, TARS1	Single nucleotide variant (synonymous variant +1 more)	TARS1-related disorder	GBenign
Select item 1334926	NM_152295.5(TARS1):c.1653G>A (p.Ala551=)	TARS1	Single nucleotide variant (synonymous variant +1 more)	TARS1-related disorder +1 more	GBenign
Select item 3056095	NM_152295.5(TARS1):c.1731-9dup	TARS1	Duplication (intron variant)	TARS1-related disorder	GBenign
Select item 3042324	NM_152295.5(TARS1):c.1738G>T (p.Gly580Cys)	TARS1 (G568C +2 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder	GBenign
Select item 769298	NM_152295.5(TARS1):c.1739G>A (p.Gly580Asp)	TARS1 (G580D +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3048199	NM_152295.5(TARS1):c.1927G>A (p.Asp643Asn)	TARS1 (D632N +2 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3045081	NM_152295.5(TARS1):c.2115C>G (p.Ile705Met)	TARS1 (I694M +2 more)	Single nucleotide variant (missense variant +1 more)	TARS1-related disorder	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 22