"Illumina Laboratory Services, Illumina"[submitter] AND "TCF4"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 327220	NM_001083962.2(TCF4):c.*5553dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327221	NM_001083962.2(TCF4):c.*5553del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327222	NM_001083962.2(TCF4):c.*5503T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889243	NM_001083962.2(TCF4):c.*5480G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889244	NM_001083962.2(TCF4):c.*5479G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889245	NM_001083962.2(TCF4):c.*5457T>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327223	NM_001083962.2(TCF4):c.*5418T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327224	NM_001083962.2(TCF4):c.*5411G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327225	NM_001083962.2(TCF4):c.5392_5393del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327226	NM_001083962.2(TCF4):c.*5383T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889919	NM_001083962.2(TCF4):c.*5370G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889920	NM_001083962.2(TCF4):c.*5369C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889921	NM_001083962.2(TCF4):c.*5339A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327227	NM_001083962.2(TCF4):c.*5319A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327228	NM_001083962.2(TCF4):c.*5299A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327229	NM_001083962.2(TCF4):c.*5240T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327230	NM_001083962.2(TCF4):c.5189_5192del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GLikely benign
Select item 891470	NM_001083962.2(TCF4):c.*5124G>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327231	NM_001083962.2(TCF4):c.*5106T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327232	NM_001083962.2(TCF4):c.*5019T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 891471	NM_001083962.2(TCF4):c.*4907G>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891472	NM_001083962.2(TCF4):c.*4833A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891473	NM_001083962.2(TCF4):c.*4789G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891474	NM_001083962.2(TCF4):c.*4752A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891475	NM_001083962.2(TCF4):c.*4623A>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327233	NM_001083962.2(TCF4):c.*4549C>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327234	NM_001083962.2(TCF4):c.*4477A>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891726	NM_001083962.2(TCF4):c.*4437G>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327235	NM_001083962.2(TCF4):c.4354_4357del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327237	NM_001083962.2(TCF4):c.4352_4353del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327236	NM_001083962.2(TCF4):c.*4353del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327238	NM_001083962.2(TCF4):c.*4338del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327241	NM_001083962.2(TCF4):c.4324_4325dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327240	NM_001083962.2(TCF4):c.*4325dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327239	NM_001083962.2(TCF4):c.4325_4326insAT	TCF4	Insertion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327242	NM_001083962.2(TCF4):c.*4325A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327243	NM_001083962.2(TCF4):c.4320_4321insGAA	TCF4	Insertion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891727	NM_001083962.2(TCF4):c.*4320A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327244	NM_001083962.2(TCF4):c.4319_4320insGA	TCF4	Insertion (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 891728	NM_001083962.2(TCF4):c.*4246G>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327245	NM_001083962.2(TCF4):c.*4214GTTTTT[3]	TCF4	Microsatellite (3 prime UTR variant)	Pitt-Hopkins syndrome +1 more	GConflicting classifications of pathogenicity
Select item 327246	NM_001083962.2(TCF4):c.*4088T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome +1 more	GBenign
Select item 327247	NM_001083962.2(TCF4):c.4081_4084del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327248	NM_001083962.2(TCF4):c.*4061dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GLikely benign
Select item 327249	NM_001083962.2(TCF4):c.*3982dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327251	NM_001083962.2(TCF4):c.3981_3982del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327250	NM_001083962.2(TCF4):c.*3982del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 891729	NM_001083962.2(TCF4):c.*3938G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327253	NM_001083962.2(TCF4):c.3868_3870del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GLikely benign
Select item 327252	NM_001083962.2(TCF4):c.*3870del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327254	NM_001083962.2(TCF4):c.*3756A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889299	NM_001083962.2(TCF4):c.*3563A>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327255	NM_001083962.2(TCF4):c.*3529T>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327256	NM_001083962.2(TCF4):c.*3491C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327257	NM_001083962.2(TCF4):c.*3418dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327258	NM_001083962.2(TCF4):c.*3404G>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome +1 more	GBenign/Likely benign
Select item 327259	NM_001083962.2(TCF4):c.*3397dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889300	NM_001083962.2(TCF4):c.*3386A>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327260	NM_001083962.2(TCF4):c.*3349C>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889301	NM_001083962.2(TCF4):c.*3338A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327261	NM_001083962.2(TCF4):c.*3269T>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889980	NM_001083962.2(TCF4):c.*3209A>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 889981	NM_001083962.2(TCF4):c.*3130C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327262	NM_001083962.2(TCF4):c.*3116C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327263	NM_001083962.2(TCF4):c.*3058C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889982	NM_001083962.2(TCF4):c.*3014C>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327264	NM_001083962.2(TCF4):c.*2989GTT[2]	TCF4	Microsatellite (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327265	NM_001083962.2(TCF4):c.*2951A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889983	NM_001083962.2(TCF4):c.*2918A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327266	NM_001083962.2(TCF4):c.*2857C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327267	NM_001083962.2(TCF4):c.*2822G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327268	NM_001083962.2(TCF4):c.2702_2704del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GLikely benign
Select item 327269	NM_001083962.2(TCF4):c.*2688A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327270	NM_001083962.2(TCF4):c.*2660A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327271	NM_001083962.2(TCF4):c.*2565T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327272	NM_001083962.2(TCF4):c.*2553C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327273	NM_001083962.2(TCF4):c.*2506G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327274	NM_001083962.2(TCF4):c.*2413G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327275	NM_001083962.2(TCF4):c.*2369TCC[2]	TCF4	Microsatellite (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891794	NM_001083962.2(TCF4):c.*2354A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891795	NM_001083962.2(TCF4):c.*2300G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891796	NM_001083962.2(TCF4):c.*2282C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327276	NM_001083962.2(TCF4):c.*2010dup	TCF4	Duplication (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327277	NM_001083962.2(TCF4):c.*2001G>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 891797	NM_001083962.2(TCF4):c.*1983T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327278	NM_001083962.2(TCF4):c.*1968TAT[1]	TCF4	Microsatellite (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891798	NM_001083962.2(TCF4):c.*1959G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891799	NM_001083962.2(TCF4):c.*1931G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 891800	NM_001083962.2(TCF4):c.*1914C>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327279	NM_001083962.2(TCF4):c.*1912A>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327280	NM_001083962.2(TCF4):c.*1903G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327281	NM_001083962.2(TCF4):c.*1889T>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889359	NM_001083962.2(TCF4):c.*1855G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327282	NM_001083962.2(TCF4):c.*1827C>T	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327283	NM_001083962.2(TCF4):c.*1799G>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 327284	NM_001083962.2(TCF4):c.*1763C>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome +1 more	GConflicting classifications of pathogenicity
Select item 327285	NM_001083962.2(TCF4):c.*1761del	TCF4	Deletion (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign
Select item 889360	NM_001083962.2(TCF4):c.*1747T>G	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 890050	NM_001083962.2(TCF4):c.*1739G>A	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GUncertain significance
Select item 327286	NM_001083962.2(TCF4):c.*1576T>C	TCF4	Single nucleotide variant (3 prime UTR variant)	Pitt-Hopkins syndrome	GBenign

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