"GeneDx"[submitter] AND "TARS2"[gene] - ClinVar

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Items: 87

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1298147	NC_000001.11:g.150487218del	TARS2	Deletion	not provided	GBenign
Select item 676423	NM_025150.4(TARS2):c.-212T>C	TARS2	Single nucleotide variant	not provided	GBenign
Select item 512315	NM_025150.4(TARS2):c.-41C>T	TARS2	Single nucleotide variant	not specified	GLikely benign
Select item 517079	NM_025150.4(TARS2):c.-31_-28del	TARS2	Deletion	not provided	GBenign
Select item 383907	NM_025150.5(TARS2):c.-22G>A	TARS2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 559355	NM_025150.5(TARS2):c.49G>A (p.Ala17Thr)	TARS2 (A17T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1258473	NM_025150.5(TARS2):c.66+136_66+139dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 680801	NM_025150.5(TARS2):c.67-166A>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 380568	NM_025150.5(TARS2):c.81C>T (p.Thr27=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 512112	NM_025150.5(TARS2):c.141A>G (p.Val47=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2663569	NM_025150.5(TARS2):c.191C>G (p.Ser64Ter)	TARS2 (S64*)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 381862	NM_025150.5(TARS2):c.263+8G>T	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 389371	NM_025150.5(TARS2):c.366C>T (p.Phe122=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GLikely benign
Select item 1178378	NM_025150.5(TARS2):c.387+199del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 680802	NM_025150.5(TARS2):c.387+238A>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 680804	NM_025150.5(TARS2):c.387+310G>T	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317641	NM_025150.5(TARS2):c.388-286C>G	TARS2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 680803	NM_025150.5(TARS2):c.388-266C>T	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227288	NM_025150.5(TARS2):c.388-174T>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 680360	NM_025150.5(TARS2):c.420G>T (p.Gly140=)	TARS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1229860	NM_025150.5(TARS2):c.512+325T>C	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250356	NM_025150.5(TARS2):c.513-331_513-330dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 1287489	NM_025150.5(TARS2):c.513-330del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 1232623	NM_025150.5(TARS2):c.513-329_513-326del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 668595	NM_025150.5(TARS2):c.513-282A>G	TARS2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 676424	NM_025150.5(TARS2):c.513-98C>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 419306	NM_025150.5(TARS2):c.513-10_513-8del	TARS2	Microsatellite (intron variant)	not provided	GBenign/Likely benign
Select item 386934	NM_025150.5(TARS2):c.562C>A (p.Leu188Ile)	TARS2 (L188I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign
Select item 2662025	NM_025150.5(TARS2):c.634A>G (p.Asn212Asp)	TARS2 (N212D)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1220777	NM_025150.5(TARS2):c.695+142del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 680807	NM_025150.5(TARS2):c.695+193C>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287997	NM_025150.5(TARS2):c.695+320_695+322dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 1278262	NM_025150.5(TARS2):c.695+321_695+322dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 1238706	NM_025150.5(TARS2):c.695+321_695+322del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 1229282	NM_025150.5(TARS2):c.695+313_695+322del	TARS2	Deletion (intron variant)	not provided	GBenign
Select item 680805	NM_025150.5(TARS2):c.696-284A>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316095	NM_025150.5(TARS2):c.722A>G (p.Gln241Arg)	TARS2 (Q241R)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 676425	NM_025150.5(TARS2):c.775-116A>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 682524	NM_025150.5(TARS2):c.900G>C (p.Arg300=)	TARS2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1220871	NM_025150.5(TARS2):c.922-30G>T	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 383915	NM_025150.5(TARS2):c.933C>G (p.Leu311=)	TARS2	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 384213	NM_025150.5(TARS2):c.1020+15G>A	TARS2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 676426	NM_025150.5(TARS2):c.1020+96C>T	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 382091	NM_025150.5(TARS2):c.1021-13C>A	TARS2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 380192	NM_025150.5(TARS2):c.1034A>G (p.His345Arg)	TARS2 (H345R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign
Select item 381177	NM_025150.5(TARS2):c.1076C>T (p.Thr359Met)	TARS2 (T359M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 512309	NM_025150.5(TARS2):c.1131C>T (p.Ala377=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GLikely benign
Select item 516719	NM_025150.5(TARS2):c.1160C>T (p.Pro387Leu)	TARS2 (P387L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2581830	NM_025150.5(TARS2):c.1175A>T (p.Asp392Val)	TARS2 (D262V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 380197	NM_025150.5(TARS2):c.1197A>G (p.Thr399=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GBenign
Select item 676427	NM_025150.5(TARS2):c.1238+73G>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 676428	NM_025150.5(TARS2):c.1238+99C>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 680808	NM_025150.5(TARS2):c.1238+255C>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 680809	NM_025150.5(TARS2):c.1238+256T>G	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 517892	NM_025150.5(TARS2):c.1239-14C>T	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 380187	NM_025150.5(TARS2):c.1251C>T (p.Ala417=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign/Likely benign
Select item 2502679	NM_025150.5(TARS2):c.1301G>A (p.Gly434Glu)	TARS2 (G304E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 380558	NM_025150.5(TARS2):c.1317C>T (p.Ala439=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related condition +2 more	GBenign
Select item 513487	NM_025150.5(TARS2):c.1353G>A (p.Leu451=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	TARS2-related condition +2 more	GLikely benign
Select item 2442666	NM_025150.5(TARS2):c.1375G>A (p.Ala459Thr)	TARS2 (A329T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 380174	NM_025150.5(TARS2):c.1401+16C>T	TARS2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 381175	NM_025150.5(TARS2):c.1401+17T>A	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1431583	NM_025150.5(TARS2):c.1439G>A (p.Arg480His)	TARS2 (R350H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 382113	NM_025150.5(TARS2):c.1453G>A (p.Val485Ile)	TARS2 (V485I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 730079	NM_025150.5(TARS2):c.1472G>A (p.Arg491His)	TARS2 (R361H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 383521	NM_025150.5(TARS2):c.1540-13C>T	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 1298065	NM_025150.5(TARS2):c.1617+90dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 1272942	NM_025150.5(TARS2):c.1617+168dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 680806	NM_025150.5(TARS2):c.1618-295G>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291457	NM_025150.5(TARS2):c.1618-25G>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 676429	NM_025150.5(TARS2):c.1719-47C>T	TARS2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1234314	NM_025150.5(TARS2):c.1719-15dup	TARS2	Duplication (intron variant)	not provided	GBenign
Select item 385038	NM_025150.5(TARS2):c.1719-20C>G	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 381421	NM_025150.5(TARS2):c.1719-17C>A	TARS2	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 511599	NM_025150.5(TARS2):c.1719-16C>A	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 383636	NM_025150.5(TARS2):c.1719-16C>T	TARS2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 432091	NM_025150.5(TARS2):c.1756C>T (p.Arg586Ter)	TARS2 (R586* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 1449004	NM_025150.5(TARS2):c.1768G>A (p.Gly590Ser)	TARS2 (G508S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1317688	NM_025150.5(TARS2):c.1812G>C (p.Gly604=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1243090	NM_025150.5(TARS2):c.1820+41G>A	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290814	NM_025150.5(TARS2):c.1894-227G>C	TARS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1800676	NM_025150.5(TARS2):c.1909C>T (p.Arg637Trp)	TARS2 (R507W +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2428824	NM_025150.5(TARS2):c.2053A>G (p.Thr685Ala)	TARS2 (T555A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 385859	NM_025150.5(TARS2):c.2103G>A (p.Gln701=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign
Select item 386359	NM_025150.5(TARS2):c.2142C>T (p.Ala714=)	TARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GLikely benign
Select item 1238582	NM_025150.5(TARS2):c.*216dup	TARS2	Duplication (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1259493	NM_025150.5(TARS2):c.*302A>G	TARS2	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

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Items: 87