"Invitae"[submitter] AND "TAF15"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 681581	NM_139215.3(TAF15):c.154G>A (p.Gly52Ser)	TAF15 (G52S)	Single nucleotide variant (missense variant)	TAF15-related condition +1 more	GLikely benign
Select item 730618	NM_139215.3(TAF15):c.365A>G (p.Tyr122Cys)	TAF15 (Y119C +1 more)	Single nucleotide variant (missense variant)	TAF15-related condition +1 more	GLikely benign
Select item 731467	NM_139215.3(TAF15):c.485-4G>C	TAF15	Single nucleotide variant (intron variant)	TAF15-related condition +1 more	GBenign/Likely benign
Select item 724070	NM_139215.3(TAF15):c.726G>A (p.Gly242=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GBenign/Likely benign
Select item 790721	NM_139215.3(TAF15):c.876C>T (p.Asp292=)	TAF15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 756136	NM_139215.3(TAF15):c.1248C>A (p.Gly416=)	TAF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 758683	NM_139215.3(TAF15):c.1314C>T (p.Ser438=)	TAF15	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 786314	NM_139215.3(TAF15):c.1347C>T (p.Asp449=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GBenign/Likely benign
Select item 786315	NM_139215.3(TAF15):c.1359T>C (p.Gly453=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GBenign/Likely benign
Select item 789091	NM_139215.3(TAF15):c.1392_1415del (p.454_461GYGGDRGG[3])	TAF15	Deletion (inframe_deletion)	TAF15-related condition +1 more	GBenign
Select item 750955	NM_139215.3(TAF15):c.1404A>C (p.Gly468=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GLikely benign
Select item 717960	NM_139215.3(TAF15):c.1422_1445del (p.454_461GYGGDRGG[3])	TAF15	Deletion (inframe_deletion)	not provided +1 more	GBenign/Likely benign
Select item 791200	NM_139215.3(TAF15):c.1446T>C (p.Asp482=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GBenign
Select item 720756	NM_139215.3(TAF15):c.1624G>A (p.Gly542Ser)	TAF15 (G542S +1 more)	Single nucleotide variant (missense variant)	TAF15-related condition +1 more	GBenign
Select item 729819	NM_139215.3(TAF15):c.1665T>A (p.Gly555=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GLikely benign
Select item 737401	NM_139215.3(TAF15):c.1668C>T (p.Gly556=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GLikely benign
Select item 786316	NM_139215.3(TAF15):c.1686A>C (p.Arg562=)	TAF15	Single nucleotide variant (synonymous variant)	TAF15-related condition +1 more	GBenign/Likely benign