"Ambry Genetics"[submitter] AND "TLE3"[gene] - ClinVar

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

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2333209	NM_001105192.3(TLE3):c.2243C>T (p.Ala748Val)	TLE3 (A739V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380095	NM_001105192.3(TLE3):c.2137G>A (p.Val713Met)	TLE3 (V706M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250068	NM_001105192.3(TLE3):c.1789A>G (p.Ile597Val)	TLE3 (I527V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248786	NM_001105192.3(TLE3):c.1661C>G (p.Thr554Ser)	TLE3 (T484S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316138	NM_001105192.3(TLE3):c.1598G>A (p.Arg533His)	TLE3 (R528H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332730	NM_001105192.3(TLE3):c.1597C>A (p.Arg533Ser)	TLE3 (R524S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326297	NM_001105192.3(TLE3):c.1468A>G (p.Thr490Ala)	TLE3 (T420A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342035	NM_001105192.3(TLE3):c.1306G>A (p.Ala436Thr)	TLE3 (A366T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326295	NM_001105192.3(TLE3):c.1274C>A (p.Pro425Gln)	TLE3 (P420Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177818	NM_001105192.3(TLE3):c.1070C>T (p.Pro357Leu)	TLE3 (P348L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570545	NM_001105192.3(TLE3):c.1055C>T (p.Ser352Leu)	TLE3 (S343L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270683	NM_001105192.3(TLE3):c.1051+3A>G	TLE3 (I352V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508970	NM_001105192.3(TLE3):c.1016C>T (p.Ser339Leu)	TLE3 (S332L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177822	NM_001105192.3(TLE3):c.973G>A (p.Asp325Asn)	TLE3 (D269N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213289	NM_001105192.3(TLE3):c.910C>T (p.Leu304Phe)	TLE3 (L248F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538647	NM_001105192.3(TLE3):c.907G>C (p.Asp303His)	TLE3 (D296H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326296	NM_001105192.3(TLE3):c.890C>T (p.Pro297Leu)	TLE3 (P290L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177821	NM_001105192.3(TLE3):c.875C>G (p.Ser292Cys)	TLE3 (S292C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241420	NM_001105192.3(TLE3):c.761A>C (p.Asn254Thr)	TLE3 (N198T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235332	NM_001105192.3(TLE3):c.754G>A (p.Val252Ile)	TLE3 (V196I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230975	NM_001105192.3(TLE3):c.646G>A (p.Gly216Ser)	TLE3 (G160S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354063	NM_001105192.3(TLE3):c.596A>G (p.Asn199Ser)	TLE3 (N199S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295498	NM_001105192.3(TLE3):c.565C>T (p.Leu189Phe)	TLE3 (L182F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352099	NM_001105192.3(TLE3):c.536C>T (p.Thr179Met)	TLE3 (T179M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177820	NM_001105192.3(TLE3):c.443C>T (p.Pro148Leu)	TLE3 (P141L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525086	NM_001105192.3(TLE3):c.442C>T (p.Pro148Ser)	TLE3 (P141S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233809	NM_001105192.3(TLE3):c.389C>T (p.Ala130Val)	TLE3 (A130V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210186	NM_001105192.3(TLE3):c.314C>T (p.Ala105Val)	TLE3 (A105V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615060	NM_001105192.3(TLE3):c.278T>C (p.Met93Thr)	TLE3 (M27T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326294	NM_001105192.3(TLE3):c.262A>G (p.Ile88Val)	TLE3 (I81V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209799	NM_001105192.3(TLE3):c.245C>T (p.Ala82Val)	TLE3 (A75V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618372	NM_001105192.3(TLE3):c.161A>G (p.Lys54Arg)	TLE3 (K54R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177819	NM_001105192.3(TLE3):c.151G>T (p.Ala51Ser)	TLE3 (A51S +1 more)	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: 33