MTSS1[gene] and "single gene"[properties] - ClinVar

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

Search results

Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296779	NM_014751.6(MTSS1):c.2242G>A (p.Asp748Asn)	MTSS1 (D666N +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296783	NM_014751.6(MTSS1):c.2140G>C (p.Glu714Gln)	MTSS1 (E649Q +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218176	NM_014751.6(MTSS1):c.2128G>A (p.Gly710Ser)	MTSS1 (G645S +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251369	NM_014751.6(MTSS1):c.2099G>C (p.Arg700Pro)	MTSS1 (R618P +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238449	NM_014751.6(MTSS1):c.2084C>G (p.Ala695Gly)	MTSS1 (A670G +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218158	NM_014751.6(MTSS1):c.2065G>A (p.Ala689Thr)	MTSS1 (A667T +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569708	NM_014751.6(MTSS1):c.1999G>A (p.Gly667Ser)	MTSS1 (G671S +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512673	NM_014751.6(MTSS1):c.1993T>G (p.Trp665Gly)	MTSS1 (W644G +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599937	NM_014751.6(MTSS1):c.1943C>T (p.Pro648Leu)	MTSS1 (P566L +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296778	NM_014751.6(MTSS1):c.1924G>A (p.Glu642Lys)	MTSS1 (E581K +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290731	NM_014751.6(MTSS1):c.1922G>A (p.Gly641Glu)	MTSS1 (G615E +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218142	NM_014751.6(MTSS1):c.1921G>A (p.Gly641Arg)	MTSS1 (G616R +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386164	NM_014751.6(MTSS1):c.1918C>T (p.Arg640Trp)	MTSS1 (R574W +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218135	NM_014751.6(MTSS1):c.1894G>C (p.Ala632Pro)	MTSS1 (A566P +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296782	NM_014751.6(MTSS1):c.1858A>G (p.Thr620Ala)	MTSS1 (T559A +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295483	NM_014751.6(MTSS1):c.1837A>G (p.Thr613Ala)	MTSS1 (T547A +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367041	NM_014751.6(MTSS1):c.1742T>C (p.Met581Thr)	MTSS1 (M515T +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409628	NM_014751.6(MTSS1):c.1733G>A (p.Gly578Glu)	MTSS1 (G496E +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216958	NM_014751.6(MTSS1):c.1697G>A (p.Arg566His)	MTSS1 (R545H +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387442	NM_014751.6(MTSS1):c.1690G>A (p.Ala564Thr)	MTSS1 (A503T +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282679	NM_014751.6(MTSS1):c.1529C>T (p.Thr510Ile)	MTSS1 (T449I +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209308	NM_014751.6(MTSS1):c.1486C>T (p.Arg496Trp)	MTSS1 (R430W +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299220	NM_014751.6(MTSS1):c.1477A>G (p.Arg493Gly)	MTSS1 (R432G +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468124	NM_014751.6(MTSS1):c.1457G>A (p.Gly486Asp)	MTSS1 (G464D +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599873	NM_014751.6(MTSS1):c.1436T>G (p.Leu479Arg)	MTSS1 (L413R +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218092	NM_014751.6(MTSS1):c.1433A>G (p.Glu478Gly)	MTSS1 (E412G +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523773	NM_014751.6(MTSS1):c.1409G>C (p.Gly470Ala)	MTSS1 (G404A +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261771	NM_014751.6(MTSS1):c.1397C>T (p.Ala466Val)	MTSS1 (A384V +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592083	NM_014751.6(MTSS1):c.1391C>T (p.Ser464Leu)	MTSS1 (S398L +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238762	NM_014751.6(MTSS1):c.1370G>A (p.Arg457Lys)	MTSS1 (R392K +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296777	NM_014751.6(MTSS1):c.1361A>C (p.Glu454Ala)	MTSS1 (E372A +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384424	NM_014751.6(MTSS1):c.1285C>T (p.Arg429Cys)	MTSS1 (R364C +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259948	NM_014751.6(MTSS1):c.1265T>A (p.Leu422Gln)	MTSS1 (L397Q +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218040	NM_014751.6(MTSS1):c.1231G>A (p.Asp411Asn)	MTSS1 (D346N +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330896	NM_014751.6(MTSS1):c.1196G>T (p.Gly399Val)	MTSS1 (G403V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218024	NM_014751.6(MTSS1):c.1186A>C (p.Ile396Leu)	MTSS1 (I395L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484334	NM_014751.6(MTSS1):c.1158C>A (p.His386Gln)	MTSS1 (H385Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604148	NM_014751.6(MTSS1):c.1111C>T (p.His371Tyr)	MTSS1 (H375Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218001	NM_014751.6(MTSS1):c.1031A>C (p.Asn344Thr)	MTSS1 (N344T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1695237	NM_014751.6(MTSS1):c.1017G>T (p.Pro339=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2213113	NM_014751.6(MTSS1):c.974T>C (p.Ile325Thr)	MTSS1 (I329T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286147	NM_014751.6(MTSS1):c.881C>T (p.Ser294Phe)	MTSS1 (S297F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658797	NM_014751.6(MTSS1):c.876G>A (p.Ser292=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3218202	NM_014751.6(MTSS1):c.875C>T (p.Ser292Leu)	MTSS1 (S295L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218200	NM_014751.6(MTSS1):c.865G>A (p.Gly289Ser)	MTSS1 (G292S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218196	NM_014751.6(MTSS1):c.856C>T (p.Arg286Trp)	MTSS1 (R285W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296781	NM_014751.6(MTSS1):c.832A>G (p.Asn278Asp)	MTSS1 (N277D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400081	NM_014751.6(MTSS1):c.830T>C (p.Leu277Pro)	MTSS1 (L281P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400941	NM_014751.6(MTSS1):c.797C>T (p.Thr266Ile)	MTSS1 (T266I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296776	NM_014751.6(MTSS1):c.691A>G (p.Met231Val)	MTSS1 (M231V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658798	NM_014751.6(MTSS1):c.483G>A (p.Gln161=)	MTSS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2494354	NM_014751.6(MTSS1):c.454A>C (p.Lys152Gln)	MTSS1 (K152Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218184	NM_014751.6(MTSS1):c.398C>T (p.Ala133Val)	MTSS1 (A133V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218179	NM_014751.6(MTSS1):c.295G>T (p.Ala99Ser)	MTSS1 (A99S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304525	NM_014751.6(MTSS1):c.263G>A (p.Ser88Asn)	MTSS1 (S88N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277139	NM_014751.6(MTSS1):c.206G>A (p.Arg69His)	MTSS1 (R69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296780	NM_014751.6(MTSS1):c.101T>C (p.Ile34Thr)	MTSS1 (I34T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464406	NM_014751.6(MTSS1):c.7G>C (p.Ala3Pro)	MTSS1 (A3P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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: 58